Aesculap, Inc.
FDA 510(k) & PMA Approved Dispositivos — 34 products
Publicidade
Total de dispositivos34
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K242762 | Aesculap Aicon® Series Container System | KCT | 2025-05-13 | Ver |
| 510(k) | K242003 | XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set | JXG | 2024-12-16 | Ver |
| 510(k) | K223596 | SQ.line KERRISON | HAE | 2023-06-29 | Ver |
| 510(k) | K214041 | Aesculap AICON Container | KCT | 2022-12-30 | Ver |
| 510(k) | K211572 | Aesculap Slim Clip Aplicador | HCI | 2021-12-13 | Ver |
| 510(k) | K203739 | ELAN 4 Electro Motor System | HBE | 2021-08-24 | Ver |
| 510(k) | K202391 | DIR 800 | IZI | 2021-01-21 | Ver |
| 510(k) | K203461 | Aesculap Caiman 12 Tecnologia de Selamento e Corte | GEI | 2020-12-18 | Ver |
| 510(k) | K202938 | Aesculap Caiman 5 Tecnologia de Selamento e Corte | GEI | 2020-10-30 | Ver |
| 510(k) | K202124 | Sistema de Anastomose Proximal PAS-Port Aesculap | FZP | 2020-09-02 | Ver |
| 510(k) | K200950 | Ventricular Catheter | JXG | 2020-05-08 | Ver |
| 510(k) | K192056 | JJ Series Container System | KCT | 2020-03-27 | Ver |
| 510(k) | K193582 | SterilContainer S2 System | KCT | 2020-03-17 | Ver |
| 510(k) | K192266 | M. Blue Adjustable Shunt System | JXG | 2019-11-21 | Ver |
| 510(k) | K183203 | ELAN 4 Tools | HBE | 2019-08-09 | Ver |
| 510(k) | K182414 | Sistema S2 SterilContainer(TM) Aesculap® | KCT | 2019-07-05 | Ver |
| 510(k) | K190174 | Miethke Shunt System GAV 2.0 and SA 2.0 Valves | JXG | 2019-07-05 | Ver |
| 510(k) | K183180 | Caiman 5 Maryland | GEI | 2019-03-12 | Ver |
| 510(k) | K182527 | ELAN 4 Tools | HBE | 2019-01-19 | Ver |
| 510(k) | K182032 | SterilContainer S System | KCT | 2018-12-21 | Ver |
Nenhum dispositivo correspondente.