GX CEPH— 510(k) K842463

Substantially Equivalent

Gendex Corp.

FDA 510(k) clearance K842463 for GX CEPH, Substantially Equivalent on 1984-08-02. 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: 1984-06-22
Decision date: 1984-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Gendex Corp.

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K925094 — VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESS1993-09-29
K931001 — ORALIX DC1993-09-14

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