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FDA 510(k), K943272, VISUALIZER 2000
FDA 510(k), K943272, VISUALIZER 2000
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510(K) Number: K943272
Device Name: VISUALIZER 2000
Manufacturer: VF-WORKS, INC.
Device Classification Name: system, x-ray, fluoroscopic, image-intensified
Regulation Number: 892.1650
Classification Product Code: JAA
Date Received: 07/07/1994
Decision Date: 12/27/1994
Regulation Medical Specialty: Radiology
Device Name: VISUALIZER 2000
Manufacturer: VF-WORKS, INC.
Device Classification Name: system, x-ray, fluoroscopic, image-intensified
Regulation Number: 892.1650
Classification Product Code: JAA
Date Received: 07/07/1994
Decision Date: 12/27/1994
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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