FDA 510(k) Applications for Medical Device Product Code "KXP"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K983045 | Owen Mumford USA, Inc. | AMIELLE | 11/25/1998 |
K202542 | PMT Corporation | Allura Vaginal Stent | 09/30/2020 |
K974479 | SILIMED, LLC. | SILIMED VAGINAL STENT | 08/05/1998 |