Mauna Kea Technologies
Dispositifs autorisés FDA 510(k) et PMA — 9 produits
Publicité
Nombre total de dispositifs9
Catégories0
Dernière décision de la FDA
| Type | Numéro | Nom du dispositif | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220477 | Cellvizio 100 series system with confocal Miniprobes | OWN | 2022-04-11 | Voir |
| 510(k) | K212322 | Cellvizio I.V.E. system with Confocal Miniprobes | OWN | 2021-08-18 | Voir |
| 510(k) | K193416 | Cellvizio I.V.E. with Confocal Miniprobes | OWN | 2020-02-28 | Voir |
| 510(k) | K191144 | Cellvizio 100 Series System with Confocal Miniprobes | OWN | 2020-01-24 | Voir |
| 510(k) | K183640 | Cellvizio 100 Series Confocal laser Imaging systems and their Confocal Miniprobes | OWN | 2019-02-22 | Voir |
| 510(k) | K180270 | Cellvizio 100 Series Systems with Confocal Miniprobes | GWG | 2018-05-22 | Voir |
| 510(k) | K172844 | Cellvizio 100 Series System with Confocal Miniprobes | OWN | 2017-12-15 | Voir |
| 510(k) | K171345 | Cellvizio 100 Series Systems with Confocal Miniprobes | OWN | 2017-08-04 | Voir |
| 510(k) | K160416 | CystoFlex UHD R-C, CelioFlex UHD 5-C, Cellvizio 100 Series (800) with Confocal Miniprobes | OWN | 2016-05-20 | Voir |
Aucun dispositif correspondant.