MODEL ELI-100/ST ELECTROCARDIOGRAPH

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MORTARA INSTRUMENT, INC.

The following data is part of a premarket notification filed by Mortara Instrument, Inc. with the FDA for Model Eli-100/st Electrocardiograph.

Pre-market Notification Details

Device IDK895232
510k NumberK895232
Device Name:MODEL ELI-100/ST ELECTROCARDIOGRAPH
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 MORTARA INSTRUMENT, INC. 7865 NORTH 86TH ST. Milwaukee,  WI  53224
ContactM Schueller
CorrespondentM Schueller
MORTARA INSTRUMENT, INC. 7865 NORTH 86TH ST. Milwaukee,  WI  53224
Product CodeLOS
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-08-21
Decision Date1989-12-13

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