The Cheney Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Cheney Co. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
The Cheney Co. has 4 FDA 510(k) cleared medical devices. Based in New Berlin, US.
Historical record: 4 cleared submissions from 1989 to 1990. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by The Cheney Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Cheney Co.
4 devices
Cleared
Jan 12, 1990
LIBERTY SPECIAL AND LIBERTY STAIRLIFTS
Physical Medicine
52d
Cleared
Jan 12, 1990
HANDI PORCH ELEVATOR
Physical Medicine
24d
Cleared
Jun 12, 1989
HANDI-LIFT/VICTORY WHEELCHAIR LIFT
Physical Medicine
39d
Cleared
Jun 12, 1989
HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT
Physical Medicine
39d