J&S Associates is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
J&S Associates - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
J&S Associates has 1 FDA 510(k) cleared medical devices. Based in Belle Mead, US.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by J&S Associates Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - J&S Associates
1 devices