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.. Device class: 2.

Clearance details

Applicant: Ocg Technology, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1981-10-22
Decision date: 1981-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Ocg Technology, Inc.

K862947 — THE EXPERT MODELS RTS 2000 AND RTS 2000H1987-11-04
K863153 — MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH1987-01-06

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