Stl International, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2016-12-30
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K162702 | Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table | HST | 2016-12-30 | View |
No matching devices.