DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM— 510(k) K852353

Name: FDA 510(k) clearance K852353
Creator: U.S. Food and Drug Administration
Published: 1985-08-07

Substantially Equivalent

Thomson-Cgr Medical Corp.

FDA 510(k) clearance K852353 for DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM, Substantially Equivalent on 1985-08-07. Applicant: Thomson-Cgr Medical Corp.. Device class: 2.

Clearance details

Applicant: Thomson-Cgr Medical Corp.
Product code: Code IXI
Device class: Class 2
Regulation: 21 CFR 892.5710
Advisory panel: Radiology
Date received: 1985-06-03
Decision date: 1985-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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