CARDIASSIST EXTERNAL COUNTERPULSATION— 510(k) K792430

Name: FDA 510(k) clearance K792430
Creator: U.S. Food and Drug Administration
Published: 1980-01-23

Substantially Equivalent

Cardiassist Corp.

FDA 510(k) clearance K792430 for CARDIASSIST EXTERNAL COUNTERPULSATION, Substantially Equivalent on 1980-01-23. Applicant: Cardiassist Corp.. Device class: 2.

Clearance details

Applicant: Cardiassist Corp.
Product code: Code DRN
Device class: Class 2
Regulation: 21 CFR 870.5225
Advisory panel: Cardiovascular
Date received: 1979-11-27
Decision date: 1980-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.