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FDA 510(k), K191419, Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire
FDA 510(k), K191419, Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire
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510(K) Number: K191419
Device Name: Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire
Manufacturer: Colin Valentis
Device Classification Name: Catheter, Peripheral, Atherectomy
Regulation Number: MCW
Classification Product Code: 05/28/2019
Date Received: 09/12/2019
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire
Manufacturer: Colin Valentis
Device Classification Name: Catheter, Peripheral, Atherectomy
Regulation Number: MCW
Classification Product Code: 05/28/2019
Date Received: 09/12/2019
Decision Date: Substantially Equivalent (SESE)
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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