MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH— 510(k) K863153

Name: FDA 510(k) clearance K863153
Creator: U.S. Food and Drug Administration
Published: 1987-01-06

Substantially Equivalent

Ocg Technology, Inc.

FDA 510(k) clearance K863153 for MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH, Substantially Equivalent on 1987-01-06. 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: 1986-08-15
Decision date: 1987-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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