MORTARA INSTRUMENT MODEL ECG PREVU— 510(k) K920377

Substantially Equivalent

Mortara Instrument, Inc.

FDA 510(k) clearance K920377 for MORTARA INSTRUMENT MODEL ECG PREVU, Substantially Equivalent on 1992-04-28. Applicant: Mortara Instrument, Inc..

Clearance details

Applicant: Mortara Instrument, Inc.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1992-01-29
Decision date: 1992-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

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