B. Braun Interventional Systems, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-06-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162625 | SeQuent Neo Percutaneous Transluminal Coronary Angioplasty (PTCA) Balloon Catheters | LOX | 2017-06-12 | View |
| 510(k) | K152765 | VENATECH CONVERTIBLE VENA CAVA FILTER SYSTEM | DTK | 2016-02-26 | View |
No matching devices.