Pmt Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2020-09-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K202542 | Allura Vaginal Stent | KXP | 2020-09-30 | View |
| 510(k) | K151790 | PMT Platinum Depthalon Depth Electrode | GZL | 2016-07-14 | View |
No matching devices.