FDA 510(k), K212725, ViperCross Support Catheters
FDA 510(k), K212725, ViperCross Support Catheters
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510(K) Number: K212725
Device Name: ViperCross Support Catheters
Manufacturer: Cardiovascular Systems, Inc.
Device Classification Name: Catheter, Percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 08/27/2021
Decision Date: 09/24/2021
Regulation Medical Specialty: Cardiovascular
Device Name: ViperCross Support Catheters
Manufacturer: Cardiovascular Systems, Inc.
Device Classification Name: Catheter, Percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 08/27/2021
Decision Date: 09/24/2021
Regulation Medical Specialty: Cardiovascular
- 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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