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FDA 510(k), K162559, Move Forward 3D Motion Simulation Service
FDA 510(k), K162559, Move Forward 3D Motion Simulation Service
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510(K) Number: K162559
Device Name: Move Forward 3D Motion Simulation Service
Manufacturer: PAUL HARDY
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 09/14/2016
Date Received: 03/31/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: Move Forward 3D Motion Simulation Service
Manufacturer: PAUL HARDY
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 09/14/2016
Date Received: 03/31/2017
Decision Date: Substantially Equivalent (SESE)
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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