Permobil of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Permobil of America - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Permobil of America has 5 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 5 cleared submissions from 1987 to 1987. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Permobil of America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Permobil of America
5 devices