P & A Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
P & A Co. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
P & A Co. has 1 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by P & A Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P & A Co.
1 devices