GX-C CEPHALOMETER— 510(k) K920189

Substantially Equivalent

Gendex Corp.

FDA 510(k) clearance K920189 for GX-C CEPHALOMETER, Substantially Equivalent on 1992-04-28. Applicant: Gendex Corp.. Device class: 2.

Clearance details

Applicant: Gendex Corp.
Product code: Code EAG
Device class: Class 2
Regulation: 21 CFR 872.1830
Advisory panel: Dental
Date received: 1992-01-15
Decision date: 1992-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Plaines, IL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.