KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC— 510(k) K943821

Substantially Equivalent

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

FDA 510(k) clearance K943821 for KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC, Substantially Equivalent on 1994-08-22. 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: 1994-06-15
Decision date: 1994-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

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