STICK-GARD STERILE CAP

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

INTEGRATED MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Integrated Medical Systems, Inc. with the FDA for Stick-gard Sterile Cap.

Pre-market Notification Details

Device IDK902682
510k NumberK902682
Device Name:STICK-GARD STERILE CAP
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 INTEGRATED MEDICAL SYSTEMS, INC. 1886 SANTA ANITA AVE. South El Monte,  CA  91733
ContactAnn L Nadler
CorrespondentAnn L Nadler
INTEGRATED MEDICAL SYSTEMS, INC. 1886 SANTA ANITA AVE. South El Monte,  CA  91733
Product CodeLDQ
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-06-19
Decision Date1990-09-26

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