FUJI HG-M INTENSIFYING SCREEN— 510(k) K943425

Substantially Equivalent

Fujifilm Medical System U.S.A., Inc.

FDA 510(k) clearance K943425 for FUJI HG-M INTENSIFYING SCREEN, Substantially Equivalent on 1994-08-17. Applicant: Fujifilm Medical System U.S.A., Inc..

Clearance details

Applicant: Fujifilm Medical System U.S.A., Inc.
Product code: Code EAM
Advisory panel: Radiology
Date received: 1994-07-15
Decision date: 1994-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

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