MEDCARE SUTURE REMOVAL KIT

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MEDCOMP TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Medcomp Technologies, Inc. with the FDA for Medcare Suture Removal Kit.

Pre-market Notification Details

Device IDK861804
510k NumberK861804
Device Name:MEDCARE SUTURE REMOVAL KIT
Classification510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products   510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la
Applicant MEDCOMP TECHNOLOGIES, INC. 2555 BAIRD RD. Penfield,  NY  14526
ContactWildeman
CorrespondentWildeman
MEDCOMP TECHNOLOGIES, INC. 2555 BAIRD RD. Penfield,  NY  14526
Product Code510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood &
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-05-09
Decision Date1986-05-23

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