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FDA 510(k), K120361, SYNAPSE 3D BASE TOOLS
FDA 510(k), K120361, SYNAPSE 3D BASE TOOLS
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510(K) Number: K120361
Device Name: SYNAPSE 3D BASE TOOLS
Manufacturer: FUJIFILM MEDICAL SYSTEMS USA, INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 02/06/2012
Decision Date: 04/06/2012
Regulation Medical Specialty: Radiology
Device Name: SYNAPSE 3D BASE TOOLS
Manufacturer: FUJIFILM MEDICAL SYSTEMS USA, INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 02/06/2012
Decision Date: 04/06/2012
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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