Jostra Medizintechnik AG
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K991864 | ROTAFLOW CENTRIFUGAL PUMP SYSTEM | KFM | 2000-08-31 | View |
| 510(k) | K001787 | QUART ARTERIAL FILTER, MODEL HBF 140 | DTM | 2000-06-30 | View |
No matching devices.
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