FDA 510(k) Applications for Medical Device Product Code "IMK"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K172601 | DEKA Research & Development Corp | Next Generation iBOT | 03/02/2018 |
K210920 | Mobius Mobility | iBOT Personal Mobility Device (iBOT PMD) | 06/16/2021 |