FDA 510(k) Applications Submitted by PMT CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151790 | 07/01/2015 | PMT Platinum Depthalon Depth Electrode | PMT CORPORATION |
| K202542 | 09/02/2020 | Allura Vaginal Stent | PMT Corporation |
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