CPE 2000 CARDIO PULMONARY ERGOMETER— 510(k) K874925

Name: FDA 510(k) clearance K874925
Creator: U.S. Food and Drug Administration
Published: 1988-01-19

Substantially Equivalent

Medical Graphics Corp.

FDA 510(k) clearance K874925 for CPE 2000 CARDIO PULMONARY ERGOMETER, Substantially Equivalent on 1988-01-19. Applicant: Medical Graphics Corp.. Device class: 1.

Clearance details

Applicant: Medical Graphics Corp.
Product code: Code KRI
Device class: Class 1
Regulation: 21 CFR 870.4200
Advisory panel: Cardiovascular
Date received: 1987-12-02
Decision date: 1988-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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