CARDIOBEEPER(R) III— 510(k) K880300

Substantially Equivalent

Survival Technology, Inc.

FDA 510(k) clearance K880300 for CARDIOBEEPER(R) III, Substantially Equivalent on 1988-05-12. Applicant: Survival Technology, Inc..

Clearance details

Applicant: Survival Technology, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1988-01-25
Decision date: 1988-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, US

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