FDA 510(k), K202752, AXS Vecta 46 Intermediate Catheter

FDA 510(k), K202752, AXS Vecta 46 Intermediate Catheter

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510(K) Number: K202752
Device Name: AXS Vecta 46 Intermediate Catheter
Manufacturer: Shivani H. Patel
Device Classification Name: Catheter, Percutaneous, Neurovasculature
Regulation Number: QJP
Classification Product Code: KXA
Date Received: 09/21/2020
Decision Date: 08/27/2021
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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