PRO BARRIER(TM) TUBE SOX(TM)

510(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

COTTRELL, LTD.

The following data is part of a premarket notification filed by Cottrell, Ltd. with the FDA for Pro Barrier(tm) Tube Sox(tm).

Pre-market Notification Details

Device IDK945575
510k NumberK945575
Device Name:PRO BARRIER(TM) TUBE SOX(TM)
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 COTTRELL, LTD. 49 PLAIN ST. North Attleboro,  MA  02760 -4153
ContactFrank S Casciani
CorrespondentFrank S Casciani
COTTRELL, LTD. 49 PLAIN ST. North Attleboro,  MA  02760 -4153
Product CodeMMN
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1994-11-14
Decision Date1995-03-06

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