OMEGA III ANGIOGRAPHIC TABLE, ROTATION & STEPPER— 510(k) K871827

Name: FDA 510(k) clearance K871827
Creator: U.S. Food and Drug Administration
Published: 1987-06-19

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K871827 for OMEGA III ANGIOGRAPHIC TABLE, ROTATION & STEPPER, Substantially Equivalent on 1987-06-19. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code KXJ
Device class: Class 2
Regulation: 21 CFR 892.1980
Advisory panel: Radiology
Date received: 1987-05-11
Decision date: 1987-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

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