Pall Medical is one of 9995 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pall Medical - FDA 510(k) Cleared Devices
Recent clearances: PALL SURGICLEAR LAPAROSCOPIC SMOKE FILTRATION SYSTEM, MODEL CLSF1, PALL DENTAL FILTRATION SYSTEM WITH AIR WATER SYRINGE HOUSING AND FILTER MEMBRANE, PALL DENTAL FILTRATION SYSTEM WITH INLINE HANDPIECE HOUSING AND FILTER MEMBRANE
6
Total
6
Cleared
0
Denied
Pall Medical has 6 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Historical record: 6 cleared submissions from 1998 to 2004.
Browse the FDA 510(k) cleared devices submitted by Pall Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pall Medical
6 devices
Cleared
Jan 22, 2004
MODIFICATION TO LAPAROSHIELD CONDITIONED INSUFFLATION SET
Obstetrics & Gynecology
30d
Cleared
May 09, 2003
LAPAROSHIELD CONDITIONED INSUFFLATION SET
Obstetrics & Gynecology
86d
Cleared
Aug 01, 2002
PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
General Hospital
318d
Cleared
Aug 20, 1999
PALL SURGICLEAR LAPAROSCOPIC SMOKE FILTRATION SYSTEM, MODEL CLSF1
General Hospital
36d
Cleared
Jan 07, 1999
PALL DENTAL FILTRATION SYSTEM WITH AIR WATER SYRINGE HOUSING AND FILTER MEMBRANE
Dental
77d
Cleared
Dec 21, 1998
PALL DENTAL FILTRATION SYSTEM WITH INLINE HANDPIECE HOUSING AND FILTER MEMBRANE
Dental
60d