Pall Corp.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K022167 | PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEM | CAC | 2003-03-07 | View |
| 510(k) | K993379 | PALL SUPOR AEF FILTER | FPB | 1999-12-16 | View |
| 510(k) | K980762 | PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE | DTM | 1998-09-01 | View |
No matching devices.
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