Pall Biomedical Products Co. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Pall Biomedical Products Co. has 28 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 28 cleared submissions from 1979 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pall Biomedical Products Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pall Biomedical Products Co.
28 devices
Cleared
Jan 09, 1997
PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER)
General Hospital
482d
Cleared
Apr 22, 1996
PALL SQ40S BLOOD FILTER (SQ40S/SQ40ST)
General Hospital
41d
Cleared
Jun 13, 1991
PALL 3N1 FILTER
General Hospital
168d
Cleared
Oct 16, 1990
LD-SIX ARTERIAL BLOOD FILTER FOR EXTRA. SERVICE
Cardiovascular
132d
Cleared
Jan 24, 1989
PALL HEPCHEK (TM) HEPARIN ABSORPTION FILTER
Hematology
88d
Cleared
Feb 29, 1988
ULTIPOR PRE-BYPASS PLUS FILTER W/POSIDYNE MEMBRANE
Cardiovascular
81d
Cleared
Feb 29, 1988
PALL CARDIOPLEGIA PLUS FILTER W/POSIDYNE MEMBRANE
Cardiovascular
81d
Cleared
Jan 06, 1988
PALL LEUKOCYTE REMOVAL FILTER, BLOOD
General Hospital
118d
Cleared
Jan 06, 1988
PALL LEUKOCYTE REMOVAL FILTER, PLATELETS
General Hospital
118d
Cleared
Dec 30, 1987
PALL STAT PRIME(TM) BLOOD FILTER FOR EXTRA. USE
Cardiovascular
63d
Cleared
Dec 11, 1985
PALL EC PLUS 3LPM MAX. FILTER W/SLEEVE
Cardiovascular
75d
Cleared
Nov 07, 1985
PALL PULMONARY FUNCTION FILTER
Anesthesiology
34d