FDR ACSELERATE SYSTEM, DR-ID 200 FLAT PANEL DETECTOR— 510(k) K093427

Substantially Equivalent

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

FDA 510(k) clearance K093427 for FDR ACSELERATE SYSTEM, DR-ID 200 FLAT PANEL DETECTOR, Substantially Equivalent on 2010-01-21. 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: 2009-11-03
Decision date: 2010-01-21
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Stamford, CT, US

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