Welch Allyn, Inc.
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) | K243598 | Welch Allyn Connex® 360 (Multiple) | 2025-07-13 | Ver | |
| 510(k) | K241411 | Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) | MWI | 2024-12-20 | Ver |
| 510(k) | K223381 | iExaminer System with Panoptic Plus | HKI | 2023-03-15 | Ver |
| 510(k) | K212473 | Welch Allyn Connex Central Station | MWI | 2022-10-28 | Ver |
| 510(k) | K191013 | Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry option | BZG | 2019-09-10 | Ver |
| 510(k) | K181016 | Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System | NFJ | 2018-07-16 | Ver |
| 510(k) | K171621 | Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor | MHX | 2017-06-30 | Ver |
Nenhum dispositivo correspondente.