ManipulatOR PRO, ManipulatOR — Gynetech Pty. , Ltd. (510(k) K150519)
ManipulatOR PRO, ManipulatOR — Gynetech Pty. , Ltd. (510(k) K150519) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ManipulatOR PRO, ManipulatOR; Applicant: Gynetech Pty. , Ltd.; Clearance track: 510(k).
| Device name | ManipulatOR PRO, ManipulatOR |
|---|---|
| Applicant | Gynetech Pty. , Ltd. |
| Clearance track | 510(k) |
| Submission number | K150519 |
| Decision | Substantially Equivalent |
| Decision date | 2015-08-19 |
| Date received | 2015-03-02 |
| Product code | LKF |
| Device class | 2 |
| Medical specialty | Obstetrics/Gynecology |
| Applicant location | AU |
| Source | openFDA device |
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