BENNETT X-RAY DIGITAL SPOT IMAGER— 510(k) K935428

Name: FDA 510(k) clearance K935428
Creator: U.S. Food and Drug Administration
Published: 1994-11-01

Substantially Equivalent

Bennett X-Ray Technologies

FDA 510(k) clearance K935428 for BENNETT X-RAY DIGITAL SPOT IMAGER, Substantially Equivalent on 1994-11-01. Applicant: Bennett X-Ray Technologies. Device class: 2.

Clearance details

Applicant: Bennett X-Ray Technologies
Product code: Code IZH
Device class: Class 2
Regulation: 21 CFR 892.1710
Advisory panel: Radiology
Date received: 1993-11-10
Decision date: 1994-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Copiague, NY, US

Download summary PDF View on FDA.gov ↗

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