Contego Medical, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2018-12-06
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181529 | Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection | LIT | 2018-12-06 | View |
| 510(k) | K181128 | Paladin Carotid Post-dilation Balloon System with Integrated Embolic Protection (Paladin System) | LIT | 2018-09-06 | View |
No matching devices.