SUPERMAX AUTOMATIC X-RAY PROCESSOR— 510(k) K760905

Name: FDA 510(k) clearance K760905
Creator: U.S. Food and Drug Administration
Published: 1976-11-19

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K760905 for SUPERMAX AUTOMATIC X-RAY PROCESSOR, Substantially Equivalent on 1976-11-19. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 1976-10-26
Decision date: 1976-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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