FCC ID LWY020051700

Medication Management System

by Aprex

Grantee Code: LWY   Product Code: 020051700
Latest application date: 1995-01-12

FCC ID Device Details

FCC IDLWY020051700
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Grantee CodeLWY
Product Code020051700
Applicant BusinessAprex 🇺🇸
Equipment ClassMedication Management System

Application Information

Application IDK9Uf16KfoT4meSVa3aRQyA==
Final Action Date1995-01-12
Application PurposeOriginal Equipment
Applicant FRN9999999999
Model020051700
Equipment ClassJBP - Part 15 Class B Computing Device Peripheral
Device DescriptionMedication Management System
Responsible PartyTom Papanek, VP of R&D;
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceNo
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationNo
Related OET Knowledge DataBase InquiryNo

Applications

Application IDDatePurpose
K9Uf16KfoT4meSVa3aRQyA==1995-01-12Original Equipment

Equipment Authorization

RulesGrant Notes
15B20, 37, CC

Grants

TCB Grant - Application K9Uf16KfoT4meSVa3aRQyA==

This application does not exist.

EAS Grant - Application K9Uf16KfoT4meSVa3aRQyA==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Aprex
1430 O'Brien Drive
Menlo Park, CA 94025
United States
  Date of Grant: 01/12/1995

Application Dated: 10/20/1994
 
Attention: Tom Papanek , VP of R&D

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:  LWY020051700
Name of Grantee:  Aprex
Equipment Class: Part 15 Class B Computing Device Peripheral
Notes: Medication Management System
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
20 37 CC 15B  - 


20: All electrical and mechanical devices employed for spurious radiation suppression, including any modifications made during certification testing, must be incorporated in each unit marketed.
37: This device has shown compliance with new rules adopted under Docket 87-389 and is not affected by Section 15.37, transition rule.
CC: This device is certified pursuant to two different Part 15 rules sections.

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