FUJI COMPUTED RADIOGRAPHY (FCR) VELOCITY IMAGE READER— 510(k) K033561

Substantially Equivalent

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

FDA 510(k) clearance K033561 for FUJI COMPUTED RADIOGRAPHY (FCR) VELOCITY IMAGE READER, Substantially Equivalent on 2003-11-26. Applicant: Fujifilm Medical System U.S.A., Inc..

Clearance details

Applicant: Fujifilm Medical System U.S.A., Inc.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2003-11-12
Decision date: 2003-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

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