Steris Corporations
FDA 510(k) & PMA Approved Dispositivos — 7 products
Publicidade
Total de dispositivos7
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K203630 | BioGuard Air/Water and Suction Valves | ODC | 2021-01-08 | Ver |
| 510(k) | K190104 | SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid Chemical Sterilant Processing System | MED | 2019-03-22 | Ver |
| 510(k) | K183295 | Celerity HP Chemical Indicator (CI) | JOJ | 2019-01-04 | Ver |
| 510(k) | K183300 | VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack | FRC | 2019-01-03 | Ver |
| 510(k) | K182931 | VERIFY All-In-One STEAM Reusable Test Pack, VERIFY All-In-One STEAM Reusable Test Pack with Step Counter, VERIFY All-In-One STEAM Reusable Test Pack with Tracker Tag | FRC | 2018-11-20 | Ver |
| 510(k) | K180342 | SYSTEM 1E Liquid Chemical Sterilant Processing System | MED | 2018-04-04 | Ver |
| 510(k) | K172748 | VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack | FRC | 2018-02-09 | Ver |
Nenhum dispositivo correspondente.