Pymah Corp., Ati Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pymah Corp., Ati Div. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Pymah Corp., Ati Div. has 3 FDA 510(k) cleared medical devices. Based in North Hollywood, US.
Historical record: 3 cleared submissions from 1989 to 1990. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pymah Corp., Ati Div. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pymah Corp., Ati Div.
3 devices