01080410 PressureWire® Aeris Test Report - FCC ID U4L01080410

FCC ID U4L01080410

Test report

PressureWire® Aeris

by St Jude Medical Systems AB

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Document Details

FCC IDU4L01080410
Document ID909003
Document TypeTest Report
DescriptionTest report
Document Title704810-2fcc
ApplicantSt Jude Medical Systems AB
Equipment ClassPressureWire® Aeris
Product Code01080410
Application IDix4slL0VbEU/idtaln2nLA==
Application PurposeOriginal Equipment
Application Date2008-03-04
Frequency Range2402-2480 MHz
FRN0016183667
Test FirmIntertek SEMKO AB
Certified ByBjörn Palmgren Regulatory Affairs Officer
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Short-Term Confidentiality Date07/09/2008
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceNo
Composite PartNo
Submitted2008-03-03
Available2008-03-04
Created2007-12-07
Modified2007-12-07
Pages21
File TypeAdobe Acrobat PDF
File Size754555
File SHA-256cc8b2aa3ff0757420f19c72c4690123327e4b63face0121e79a4282f653413c8
PDF Metadata Authorsandersson
PDF Metadata CreatorPScript5.dll Version 5.2.2
PDF Metadata ProducerAcrobat Distiller 7.0.5 (Windows)
FCC.gov SourcesFCC.gov 909003

Related FCC Exhibits

DocumentTypeAvailableFile
Users manualUsers Manual2008-07-09PDF 277.9 KB
External photosExternal Photos2008-07-09PDF 36.3 KB
Label and location infoID Label/Location Info2008-03-04PDF 72.2 KB
Test setup photosTest Setup Photos2008-07-09PDF 104 KB
Test reportTest Report2008-03-04PDF 736.9 KB
Authorization letterCover Letter(s)2008-03-04PDF 224.5 KB
Confidentiality requestCover Letter(s)2008-03-04PDF 628.2 KB