PERCUTANEOUS TRACHEOSTOMY DEVICE

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FREDERIC J. TOYE, M.D.

The following data is part of a premarket notification filed by Frederic J. Toye, M.d. with the FDA for Percutaneous Tracheostomy Device.

Pre-market Notification Details

Device IDK821821
510k NumberK821821
Device Name:PERCUTANEOUS TRACHEOSTOMY DEVICE
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 FREDERIC J. TOYE, M.D. 4221 Richmond Rd., N.W. Walker,  MI  49534
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 Received1982-06-22
Decision Date1982-07-19

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