BENNETT X-RAY ID PLUS— 510(k) K925332

Name: FDA 510(k) clearance K925332
Creator: U.S. Food and Drug Administration
Published: 1992-11-27

Substantially Equivalent

Bennett X-Ray Technologies

FDA 510(k) clearance K925332 for BENNETT X-RAY ID PLUS, Substantially Equivalent on 1992-11-27. Applicant: Bennett X-Ray Technologies. Device class: 1.

Clearance details

Applicant: Bennett X-Ray Technologies
Product code: Code JAC
Device class: Class 1
Regulation: 21 CFR 892.1640
Advisory panel: Radiology
Date received: 1992-10-21
Decision date: 1992-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Copiague, NY, US

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