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FDA 510(k), K132904, ZIEHM VISION RFD
FDA 510(k), K132904, ZIEHM VISION RFD
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510(K) Number: K132904
Device Name: ZIEHM VISION RFD
Manufacturer: ZIEHM IMAGING GMBH
Device Classification Name: System, X-Ray, Fluoroscopic, Image-Intensified
Regulation Number: 892.1650
Classification Product Code: JAA
Date Received: 09/16/2013
Decision Date: 12/05/2013
Regulation Medical Specialty: Radiology
Device Name: ZIEHM VISION RFD
Manufacturer: ZIEHM IMAGING GMBH
Device Classification Name: System, X-Ray, Fluoroscopic, Image-Intensified
Regulation Number: 892.1650
Classification Product Code: JAA
Date Received: 09/16/2013
Decision Date: 12/05/2013
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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