Merit Medical Ireland , Ltd.
FDA 510(k) & PMA Approved Dispositivos — 5 products
Publicidade
Total de dispositivos5
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K261640 | Merit MAK Nitinol/Gold-Tungsten Guide Wire | DQX | 2026-07-13 | Ver |
| 510(k) | K254137 | InQwire Amplatz Guide Wire | DQX | 2026-05-22 | Ver |
| 510(k) | K253847 | Splashwire Hydrophilic Guide Wire (MSWSTD35150J3) | DQX | 2026-01-31 | Ver |
| 510(k) | K251385 | InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S) | DQX | 2026-01-21 | Ver |
| 510(k) | K251181 | Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guide Wire (MSWSTD35260J1O5); Splashwire Hydrophilic Guide Wire (MSWSTDA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35260LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFS38150LT) | DQX | 2025-08-29 | Ver |
Nenhum dispositivo correspondente.