Burke Mobility Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Burke Mobility Products - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Burke Mobility Products has 3 FDA 510(k) cleared medical devices. Based in Kansas City, US.
Historical record: 3 cleared submissions from 1990 to 1996. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Burke Mobility Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Burke Mobility Products
4 devices
Cleared
Mar 19, 1996
PACE SAVER LITTLE JUNIOR (MODIFICATION)
Physical Medicine
146d
Cleared
Mar 30, 1994
PACE SAVER LITTLE JR
Physical Medicine
537d
Cleared
Jun 04, 1993
BURKE BARIATRIC TREATMENT SYSTEM II
General Hospital
213d
Cleared
Feb 22, 1990
BOOSTER MOTORIZED THREE WHEELED VEHICLE
Physical Medicine
6d