CARDIOTRAK— 510(k) K802089

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K802089 for CARDIOTRAK, Substantially Equivalent on 1980-09-26. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1980-09-02
Decision date: 1980-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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