FDA 510(k) Applications Submitted by PALL CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K022167 07/03/2002 PALL DONER PRE-EVACUATED POST-OPERATIVE AUTOLOGOUS BLOOD REINFUSION SYSTEM PALL CORP.
K993379 10/07/1999 PALL SUPOR AEF FILTER PALL CORP.
K980762 02/27/1998 PALL STAT-PRIME D BLOOD FILTER FOR EXTRACORPOREAL SERVICE PALL CORP.


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