APOLLO HEART RATE INDICATOR— 510(k) K790999

Name: FDA 510(k) clearance K790999
Creator: U.S. Food and Drug Administration
Published: 1979-06-22

Substantially Equivalent

Apollo Products, Inc.

FDA 510(k) clearance K790999 for APOLLO HEART RATE INDICATOR, Substantially Equivalent on 1979-06-22. Applicant: Apollo Products, Inc.. Device class: 2.

Clearance details

Applicant: Apollo Products, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1979-05-29
Decision date: 1979-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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