Preanalytix GmbH
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) | K231469 | PAXgene® Blood DNA Tube | PJE | 2023-06-21 | View |
| 510(k) | K082150 | MODIFICATION TO PAXGENE BLOOD RNA SYSTEM | NTW | 2009-02-04 | View |
No matching devices.
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