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FDA 510(k), K202610, Ventrax Delivery System
FDA 510(k), K202610, Ventrax Delivery System
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$149.00 USD
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510(K) Number: K202610
Device Name: Ventrax Delivery System
Manufacturer: Merit Medical Systems, Inc.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 09/09/2020
Decision Date: 12/14/2020
Regulation Medical Specialty: Cardiovascular
Device Name: Ventrax Delivery System
Manufacturer: Merit Medical Systems, Inc.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 09/09/2020
Decision Date: 12/14/2020
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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