Js & A Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Js & A Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Js & A Group has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1980 to 1980. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Js & A Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Js & A Group
2 devices