Axess Vision Technology
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-02-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212886 | Broncoflex Agile, Broncoflex Vortex, Screeni | EOQ | 2022-02-16 | View |
| 510(k) | K202180 | Broncoflex Agile; Product Reference: 20030001 , Broncoflex Vortex; Product Reference: 10030001, Screeni; Product Reference: 30030001 | EOQ | 2020-10-22 | View |
No matching devices.