Catheter, Angioplasty, Peripheral, Transluminal, Dual-balloon — FDA 510(k) Devices
Percutaneous Transluminal Angioplasty Of Peripheral Vasculature Exclusive Of Coronary Arteries
2
Total
2
Cleared
35d
Avg days
2021
Since
List of Catheter, Angioplasty, Peripheral, Transluminal, Dual-balloon devices cleared through 510(k)
2 devices
Cleared
Jan 12, 2022
BIB Stent Placement Catheter
NuMED, Inc.
Cardiovascular
28d
Cleared
May 27, 2021
BIB Stent Placement Catheter
NuMED, Inc.
Cardiovascular
41d
How to use this database
This page lists all FDA 510(k) submissions for Catheter, Angioplasty, Peripheral, Transluminal, Dual-balloon devices (product code NVM). Click any device to view full submission details, including the decision date, manufacturer information, predicate device, and a link to the official FDA record.
These devices fall under the Cardiovascular FDA review panel. Browse all Cardiovascular devices →