SECHRIST VOLUME VENTILATOR MODIFICATION

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SECHRIST INDUSTRIES, INC.

The following data is part of a premarket notification filed by Sechrist Industries, Inc. with the FDA for Sechrist Volume Ventilator Modification.

Pre-market Notification Details

Device IDK850740
510k NumberK850740
Device Name:SECHRIST VOLUME VENTILATOR MODIFICATION
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 SECHRIST INDUSTRIES, INC. 2820 GRETTA LN. Anaheim,  CA  92806
ContactEdwin Weninger
CorrespondentEdwin Weninger
SECHRIST INDUSTRIES, INC. 2820 GRETTA LN. Anaheim,  CA  92806
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 Received1985-01-28
Decision Date1985-07-29

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