MicroVention, Inc. A TERUMO Group Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
MicroVention, Inc. A TERUMO Group Company - FDA 510(k) Cleared Devices
Recent clearances: PG Pro Microcatheter
1
Total
1
Cleared
0
Denied
MicroVention, Inc. A TERUMO Group Company has 1 FDA 510(k) cleared medical devices. Based in Aliso Veijo, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by MicroVention, Inc. A TERUMO Group Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - MicroVention, Inc. A TERUMO Group Company
1 devices