GE-700 INTRA ORAL X-RAY SYSTEM— 510(k) K781630

Name: FDA 510(k) clearance K781630
Creator: U.S. Food and Drug Administration
Published: 1978-12-04

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K781630 for GE-700 INTRA ORAL X-RAY SYSTEM, Substantially Equivalent on 1978-12-04. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code EAP
Device class: Class 2
Regulation: 21 CFR 872.1810
Advisory panel: Dental
Date received: 1978-09-25
Decision date: 1978-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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