FDA 510(k) Applications Submitted by The O R Company Pty Ltd
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212505 | 08/09/2021 | DUMI ManipulatOR | The O R Company Pty Ltd |
| K220202 | 01/24/2022 | Uterine ElevatOR PRO with OccludOR Balloon | The O R Company Pty Ltd |
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