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.. Device class: 2.

Clearance details

Applicant
Cardiac Pacemakers, Inc.
Product code
Code DTA
Device class
Class 2
Regulation
21 CFR 870.3720
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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