MODEL 410 DENTAL X-RAY FILM PROCESSORS— 510(k) K874118

Name: FDA 510(k) clearance K874118
Creator: U.S. Food and Drug Administration
Published: 1987-11-06

Substantially Equivalent

Dent-X Co.

FDA 510(k) clearance K874118 for MODEL 410 DENTAL X-RAY FILM PROCESSORS, Substantially Equivalent on 1987-11-06. Applicant: Dent-X Co.. Device class: 2.

Clearance details

Applicant: Dent-X Co.
Product code: Code EGY
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 1987-10-09
Decision date: 1987-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elmsford, NY, US

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