Hydrocision, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2025-07-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241990 | SpineSite Endoscope System | HRX | 2025-07-30 | View |
| 510(k) | K200729 | HydroCision SpineJet System | HRX | 2020-04-16 | View |
| 510(k) | K190804 | HydroCision TenJet Device | HRX | 2019-06-05 | View |
No matching devices.