Medical Device Manufacturer · US , Ann Arbor , MI

Pall Medical - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Recent clearances: MODIFICATION TO LAPAROSHIELD CONDITIONED INSUFFLATION SET, LAPAROSHIELD CONDITIONED INSUFFLATION SET, PALL ULTIPOR ANESTHESIA BREATHING SYSTEM

View 6 510(k) Devices ↓

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.

Pall Medical is one of 23557 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pall Medical

6 devices

1-6 of 6

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

Cleared Dec 21, 1998

PALL DENTAL FILTRATION SYSTEM WITH INLINE HANDPIECE HOUSING AND FILTER MEMBRANE