Rist Neurovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rist Neurovascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RIST Radial Access Catheter, RIST Radial Access Catheter, RIST Cath Radial Access Long Sheath
3
Total
3
Cleared
0
Denied
Rist Neurovascular, Inc. has 3 FDA 510(k) cleared medical devices. Based in Miramar, US.
Historical record: 3 cleared submissions from 2019 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Rist Neurovascular, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Caraballo Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Rist Neurovascular, Inc.
3 devices