GENERATOR, HIGH VOLT, X-RAY, MPX 125— 510(k) K802550

Name: FDA 510(k) clearance K802550
Creator: U.S. Food and Drug Administration
Published: 1980-12-02

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K802550 for GENERATOR, HIGH VOLT, X-RAY, MPX 125, Substantially Equivalent on 1980-12-02. Applicant: General Electric Co.. Device class: 1.

Clearance details

Applicant: General Electric Co.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1980-10-15
Decision date: 1980-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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