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FDA 510(k), K171392, ulrichINJECT CT motion
FDA 510(k), K171392, ulrichINJECT CT motion
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510(K) Number: K171392
Device Name: ulrichINJECT CT motion
Manufacturer: ulrich GmbH & Co. KG
Device Classification Name: Injector, Contrast Medium, Automatic
Regulation Number: 870.1650
Classification Product Code: IZQ
Date Received: 05/11/2017
Decision Date: 11/09/2017
Regulation Medical Specialty: Cardiovascular
Device Name: ulrichINJECT CT motion
Manufacturer: ulrich GmbH & Co. KG
Device Classification Name: Injector, Contrast Medium, Automatic
Regulation Number: 870.1650
Classification Product Code: IZQ
Date Received: 05/11/2017
Decision Date: 11/09/2017
Regulation Medical Specialty: Cardiovascular
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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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