CARDIOTEST 2200— 510(k) K790503

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K790503 for CARDIOTEST 2200, Substantially Equivalent on 1979-05-17. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code DTA
Advisory panel: Cardiovascular
Date received: 1979-03-13
Decision date: 1979-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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