Intersect Ent. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intersect Ent. - FDA 510(k) Cleared Devices
Recent clearances: VenSure LightGuide
1
Total
1
Cleared
0
Denied
Intersect Ent. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Intersect Ent. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intersect Ent.
1 devices