FUJI MEDICAL LASER IMAGER— 510(k) K900885

Substantially Equivalent

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

FDA 510(k) clearance K900885 for FUJI MEDICAL LASER IMAGER, Substantially Equivalent on 1990-03-23. Applicant: Fujifilm Medical System U.S.A., Inc..

Clearance details

Applicant: Fujifilm Medical System U.S.A., Inc.
Product code: Code LMC
Advisory panel: Radiology
Date received: 1990-02-26
Decision date: 1990-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

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