DIAGNOSTIC MICROSOPCE SLIDES

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SYBRON CORP.

The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Diagnostic Microsopce Slides.

Pre-market Notification Details

Device IDK844092
510k NumberK844092
Device Name:DIAGNOSTIC MICROSOPCE SLIDES
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 SYBRON CORP. Portsmouth,  NH  03801
ContactHenry N Williams
CorrespondentHenry N Williams
SYBRON CORP. Portsmouth,  NH  03801
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 Received1984-10-19
Decision Date1984-10-25

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