MAYO-HEGAR NEEDLE HOLDER

Guide, Needle, Surgical

CONPHAR, INC.

The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Mayo-hegar Needle Holder.

Pre-market Notification Details

Device IDK821289
510k NumberK821289
Device Name:MAYO-HEGAR NEEDLE HOLDER
ClassificationGuide, Needle, Surgical
Applicant CONPHAR, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGDF  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-05-04
Decision Date1982-06-03

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