Pall Corp.
FDA Regulatory Profile
Pall Corp. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 7, 2003.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K022167 | PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEM | March 7, 2003 |
| K993379 | PALL SUPOR AEF FILTER | December 16, 1999 |
| K980762 | PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE | September 1, 1998 |