SURGICAL STARTER KIT

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DEVON INDUSTRIES, INC.

The following data is part of a premarket notification filed by Devon Industries, Inc. with the FDA for Surgical Starter Kit.

Pre-market Notification Details

Device IDK870744
510k NumberK870744
Device Name:SURGICAL STARTER 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 DEVON INDUSTRIES, INC. 9530 DESOTO AVE. Chatsworth,  CA  91311
ContactRobert T Horan
CorrespondentRobert T Horan
DEVON INDUSTRIES, INC. 9530 DESOTO AVE. Chatsworth,  CA  91311
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 - With Drug (SESD)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-02-25
Decision Date1987-04-10

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