FDA 510(k), K214048, Millipede 088 Access Catheter
FDA 510(k), K214048, Millipede 088 Access Catheter
Device Name: Millipede 088 Access Catheter
Manufacturer: Anne-Marie Gannon
Device Classification Name: Catheter, Percutaneous, Neurovasculature
Regulation Number: QJP
Classification Product Code: KXA
Date Received: 12/27/2021
Decision Date: 09/20/2022
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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