FUJIFILM TOMOSYNTHESIS OPTION FOR FDR ACSELERATE STATIONARY X-RAY SYSTEM— 510(k) K121499

Substantially Equivalent

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

FDA 510(k) clearance K121499 for FUJIFILM TOMOSYNTHESIS OPTION FOR FDR ACSELERATE STATIONARY X-RAY SYSTEM, Substantially Equivalent on 2012-11-20. Applicant: Fujifilm Medical System U.S.A., Inc..

Clearance details

Applicant: Fujifilm Medical System U.S.A., Inc.
Product code: Code IZF
Advisory panel: Radiology
Date received: 2012-05-21
Decision date: 2012-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

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