Applied Medical Resources Corp.
FDA 510(k) & PMA Approved Produkte — 11 products
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Produkte insgesamt11
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Neueste FDA-Entscheidung
| Typ | Nummer | Produktname | Code | Datum | Aktionen |
|---|---|---|---|---|---|
| 510(k) | K252740 | Voyant® Open Fusion Device (EB240/Open Fusion) | GEI | 2025-11-04 | Anzeigen |
| 510(k) | K252442 | Kii Structural Balloon Access System | GCJ | 2025-10-31 | Anzeigen |
| 510(k) | K243152 | GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device | HEW | 2025-10-02 | Anzeigen |
| 510(k) | K201212 | Voyant Open Fusion Device | GEI | 2020-06-05 | Anzeigen |
| 510(k) | K200598 | Voyant Maryland Fusion Device | GEI | 2020-04-08 | Anzeigen |
| 510(k) | K193292 | Voyant 5mm Fusion Device, Voyant Maryland Fusion Device | GEI | 2019-12-20 | Anzeigen |
| 510(k) | K191294 | Transvaginal Access Platform | HEW | 2019-09-06 | Anzeigen |
| 510(k) | K182653 | Voyant Maryland Fusion Device | GEI | 2018-11-14 | Anzeigen |
| 510(k) | K182244 | Voyant Electrosurgical Generator | GEI | 2018-10-11 | Anzeigen |
| 510(k) | K182024 | Dissecting Balloon System | GCJ | 2018-08-30 | Anzeigen |
| 510(k) | K171701 | GelPOINT Path Transanal Access Platform | FER | 2017-07-20 | Anzeigen |
Keine passenden Geräte.