HEMORRHOIDAL FORCEPS

Forceps

KINETIC MEDICAL PRODUCTS

The following data is part of a premarket notification filed by Kinetic Medical Products with the FDA for Hemorrhoidal Forceps.

Pre-market Notification Details

Device IDK890373
510k NumberK890373
Device Name:HEMORRHOIDAL FORCEPS
ClassificationForceps
Applicant KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie,  PA  16509
ContactJames I Laughner
CorrespondentJames I Laughner
KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie,  PA  16509
Product CodeHTD  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-01-23
Decision Date1989-02-03

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