Ki Mobility, LLC
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest Approval2023-09-05
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K200583 | Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL | IOR | 2023-09-05 | View |
| 510(k) | K201869 | Ki Power Tilt System | ITI | 2023-09-05 | View |
| 510(k) | K223533 | Little Wave Arc; Little Wave Flip | LBE | 2023-08-31 | View |
| 510(k) | K223527 | Little Wave Clik, Rogue XP, Little Wave XP, Spark | IOR | 2023-08-31 | View |
No matching devices.