Philips Healthcare (Suzhou) Co., Ltd.
FDA 510(k) & PMA Approved Dispositivos — 16 products
Publicidade
Total de dispositivos16
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K252992 | CT Rembra RT; CT Areta RT; CT Rembra | JAK | 2026-03-23 | Ver |
| 510(k) | K260519 | Smart Fit TorsoCardiac 1.5T | MOS | 2026-03-20 | Ver |
| 510(k) | K242329 | CT Collaboration Live | LLZ | 2024-11-18 | Ver |
| 510(k) | K232491 | CT 5300 | JAK | 2024-05-03 | Ver |
| 510(k) | K233600 | Smart Fit Knee 3.0T | MOS | 2024-02-05 | Ver |
| 510(k) | K232021 | Smart Fit TorsoCardiac 1.5T and Smart Fit Shoulder 1.5T | MOS | 2023-09-01 | Ver |
| 510(k) | K223311 | Philips CT 3500 | JAK | 2022-12-22 | Ver |
| 510(k) | K212441 | Philips Incisive CT | JAK | 2022-04-27 | Ver |
| 510(k) | K212864 | dS TorsoCardiac 1.5T, dS MSK S 1.5T, dS MSK M 1.5T | MOS | 2021-12-01 | Ver |
| 510(k) | K211168 | Philips Incisive CT on Trailer | JAK | 2021-11-22 | Ver |
| 510(k) | K203514 | Precise Position | JAK | 2021-06-17 | Ver |
| 510(k) | K201640 | DuraDiagnost | KPR | 2020-07-09 | Ver |
| 510(k) | K191136 | Access CT | JAK | 2019-07-29 | Ver |
| 510(k) | K173507 | Prodiva 1.5T CX and Prodiva 1.5T CS R5.4 | LNH | 2018-06-15 | Ver |
| 510(k) | K180015 | Philips Incisive CT | JAK | 2018-03-20 | Ver |
| 510(k) | K163410 | DigitalDiagnost C50 | KPR | 2017-01-04 | Ver |
Nenhum dispositivo correspondente.