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Pall Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K022167PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEMMarch 7, 2003
K993379PALL SUPOR AEF FILTERDecember 16, 1999
K980762PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICESeptember 1, 1998