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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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