CARDIOINTEGRAM— 510(k) K812971

Substantially Equivalent

Ocg Technology, Inc.

FDA 510(k) clearance K812971 for CARDIOINTEGRAM, Substantially Equivalent on 1981-12-29. Applicant: Ocg Technology, Inc..

Clearance details

Applicant: Ocg Technology, Inc.
Product code: Code DXG
Advisory panel: Cardiovascular
Date received: 1981-10-22
Decision date: 1981-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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