ARTHROSCOPY LEG HOLDER

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

EDER INSTRUMENT CO, INC.

The following data is part of a premarket notification filed by Eder Instrument Co, Inc. with the FDA for Arthroscopy Leg Holder.

Pre-market Notification Details

Device IDK843499
510k NumberK843499
Device Name:ARTHROSCOPY LEG HOLDER
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 EDER INSTRUMENT CO, INC. 735 NORTH WATER ST. SUITE 1102 Milwaukee, Wi 53202,  53202
ContactDaniel D Fetterley
CorrespondentDaniel D Fetterley
EDER INSTRUMENT CO, INC. 735 NORTH WATER ST. SUITE 1102 Milwaukee, Wi 53202,  53202
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 Received1984-09-06
Decision Date1984-10-31

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.