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FDA 510(k) Applications for Medical Device Product Code "IMK"
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| 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 |
| K243442 | Mobius Mobility | iBOT« PMD | 01/30/2025 |