COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER

Catheter, Assisted Reproduction

COOPER SURGICAL

The following data is part of a premarket notification filed by Cooper Surgical with the FDA for Coopersurgical Intrauterine Insemination Catheter.

Pre-market Notification Details

Device IDK023383
510k NumberK023383
Device Name:COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER
ClassificationCatheter, Assisted Reproduction
Applicant COOPER SURGICAL P.O. BOX 2156 Huntington,  CT  06484
ContactJoseph M Azary
CorrespondentJoseph M Azary
COOPER SURGICAL P.O. BOX 2156 Huntington,  CT  06484
Product CodeMQF  
CFR Regulation Number884.6110 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-10-08
Decision Date2002-12-13
Summary:summary

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.