MAXICAMERA 400T W/BODY CONTOUR TOMOGRA— 510(k) K841996

Name: FDA 510(k) clearance K841996
Creator: U.S. Food and Drug Administration
Published: 1984-07-16

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K841996 for MAXICAMERA 400T W/BODY CONTOUR TOMOGRA, Substantially Equivalent on 1984-07-16. Applicant: General Electric Co.. Device class: 1.

Clearance details

Applicant: General Electric Co.
Product code: Code JAM
Device class: Class 1
Regulation: 21 CFR 892.1330
Advisory panel: Radiology
Date received: 1984-05-16
Decision date: 1984-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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