FCC ID QBI-1014

C5 Ambulatory ECG Monitoring System

by Cardionet

Grantee Code: QBI   Product Code: 1014
Latest application date: 2016-08-31

Device Images

FCC ID Device Details

FCC IDQBI-1014
Mirrorsfcc.id | gov | fccid.ai
Grantee CodeQBI
Product Code1014
Applicant BusinessCardionet 🇺🇸
Related Domains cardionet.com
Equipment ClassC5 Ambulatory ECG Monitoring System
Test FirmTUV SUD America, Inc.

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
902.96-926.28 MHzOriginal Equipment2016-08-31

Exhibits

DocumentTypeAvailableFile
ManualUsers Manual2016-08-31PDF 2.5 MB
Internal PhotosInternal Photos2016-08-31PDF 802.3 KB
External PhotosExternal Photos2016-08-31PDF 406.5 KB
Label InformationID Label/Location Info2016-08-31PDF 1 MB
Test Setup PhotosTest Setup Photos2016-08-31PDF 1 MB
Test ReportTest Report2016-08-31PDF 550.4 KB
Agency AgreementCover Letter(s)2016-08-31PDF 47.2 KB
Confidentiality RequestCover Letter(s)2016-08-31PDF 22.8 KB
FCC Cover LetterCover Letter(s)2016-08-31PDF 22.8 KB
SAR ReportRF Exposure Info2016-08-31PDF 2.4 MB
Block Diagram Metadata onlyBlock DiagramPDF 106.3 KB
Schematics Metadata onlySchematicsPDF 1.1 MB
Theory of Operation Metadata onlyOperational DescriptionPDF 320.3 KB

Application Information

Application IDiD6WQxJqeDucCDGQu7c4PQ==
Final Action Date2016-08-31
Application PurposeOriginal Equipment
Applicant FRN0006907885
Model1014
Frequency Range902.96-926.28 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionC5 Ambulatory ECG Monitoring System
Responsible PartyKent Sayler, Quality/Regulatory VP, kent.sayler@cardionet.com , 619 243 7560
AgentSam Sam Sam, Advanced Compliance Solutions, Inc.
Test FirmSam Wismer, TUV SUD America, Inc., swismer@tuvam.com , 678-341-5924
TCB Emailjwoods@acstestlab.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityYes
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceNo
Composite PartYes
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsPower listed is conducted. The antenna(s) used in this device must not be co-located or operated in conjunction with any other antenna or transmitter except as described in this filing. End-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. Device is approved for body-worn condition only. Device is co-located with FCC ID: RI7CE910-DUAL and FCC ID: Q2331308. Device is exempt from stand-alone use; the highest reported SAR for simultaneous transmission exposure conditions is 1.37 W/kg.

Applications

Application IDDatePurpose
iD6WQxJqeDucCDGQu7c4PQ==2016-08-31Original Equipment

Equipment Authorization

FrequencyOutputRules
902.96-926.28 MHz0.010900015C

Grants

TCB Grant - Application iD6WQxJqeDucCDGQu7c4PQ==

TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  TUV SUD America Inc.
401 Edgewater Place Suite #500
Wakefield, MA 01880
Date of Grant: 08/31/2016

Application Dated: 08/31/2016
Cardionet
3890 Murphy Canyon Rd
Suite 100
San Diego, CA 92123
 
Attention: Kent Sayler , Quality/Regulatory VP

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  QBI-1014
Name of Grantee:  Cardionet
Equipment Class: Digital Transmission System
Notes: C5 Ambulatory ECG Monitoring System
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 902.96  -  926.28 0.0109  

Power listed is conducted. The antenna(s) used in this device must not be co-located or operated in conjunction with any other antenna or transmitter except as described in this filing. End-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. Device is approved for body-worn condition only. Device is co-located with FCC ID: RI7CE910-DUAL and FCC ID: Q2331308. Device is exempt from stand-alone use; the highest reported SAR for simultaneous transmission exposure conditions is 1.37 W/kg.

EAS Grant - Application iD6WQxJqeDucCDGQu7c4PQ==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Cardionet
3890 Murphy Canyon Rd Suite 100
San Diego, CA 92123
United States
  Date of Grant: 08/31/2016

Application Dated: 08/31/2016
 
Attention: Kent Sayler , Quality/Regulatory VP

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  QBI-1014
Name of Grantee:  Cardionet
Equipment Class: Digital Transmission System
Notes: C5 Ambulatory ECG Monitoring System
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 902.96  -  926.28 0.0109  

Power listed is conducted. The antenna(s) used in this device must not be co-located or operated in conjunction with any other antenna or transmitter except as described in this filing. End-users must be provided with transmitter operating conditions for satisfying RF exposure compliance. Device is approved for body-worn condition only. Device is co-located with FCC ID: RI7CE910-DUAL and FCC ID: Q2331308. Device is exempt from stand-alone use; the highest reported SAR for simultaneous transmission exposure conditions is 1.37 W/kg.



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