Disccath, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Disccath, LLC - FDA 510(k) Cleared Devices
Recent clearances: DiscCath Needle Set
1
Total
1
Cleared
0
Denied
Disccath, LLC has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Disccath, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Disccath, LLC
1 devices