SOPHER AND BIERER OVUM FORCEPS

Electrode, Corneal

THOMASVILLE MEDICAL ASSOC.

The following data is part of a premarket notification filed by Thomasville Medical Assoc. with the FDA for Sopher And Bierer Ovum Forceps.

Pre-market Notification Details

Device IDK926540
510k NumberK926540
Device Name:SOPHER AND BIERER OVUM FORCEPS
ClassificationElectrode, Corneal
Applicant THOMASVILLE MEDICAL ASSOC. 935 COBBLESTONE COURT Alpharetta,  GA  30201
ContactThomas J Zinnanti
CorrespondentThomas J Zinnanti
THOMASVILLE MEDICAL ASSOC. 935 COBBLESTONE COURT Alpharetta,  GA  30201
Product CodeHLZ  
CFR Regulation Number886.1220 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-12-30
Decision Date1994-02-25

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