ALLIGATOR CUP FORCEPS

Forceps, Ent

EDWARD WECK, INC.

The following data is part of a premarket notification filed by Edward Weck, Inc. with the FDA for Alligator Cup Forceps.

Pre-market Notification Details

Device IDK772396
510k NumberK772396
Device Name:ALLIGATOR CUP FORCEPS
ClassificationForceps, Ent
Applicant EDWARD WECK, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKAE  
CFR Regulation Number874.4420 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1977-12-27
Decision Date1978-01-17

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