E-FAX RECEIVER

Transmitters And Receivers, Electrocardiograph, Telephone

COHERENT SYSTEMS, INC.

The following data is part of a premarket notification filed by Coherent Systems, Inc. with the FDA for E-fax Receiver.

Pre-market Notification Details

Device IDK932859
510k NumberK932859
Device Name:E-FAX RECEIVER
ClassificationTransmitters And Receivers, Electrocardiograph, Telephone
Applicant COHERENT SYSTEMS, INC. 1000 BAY AREA BLVD. SUITE 206 Houston,  TX  77058
ContactTommy Cooper
CorrespondentTommy Cooper
COHERENT SYSTEMS, INC. 1000 BAY AREA BLVD. SUITE 206 Houston,  TX  77058
Product CodeDXH  
CFR Regulation Number870.2920 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-06-11
Decision Date1994-02-24

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