Bd Kiestra B.V.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2023-05-04
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213280 | BD Kiestra Methicillin-resistant Staphylococcus aureus (MRSA) Application, BD Kiestra MRSA App | QQY | 2023-05-04 | View |
No matching devices.