Karmelsonix is one of 489 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Karmelsonix - FDA 510(k) Cleared Devices
Recent clearances: PULMOTRACK 2020 SYSTEM, PULMOTRACK 5050 WHOLTER, MODEL 5050, PERSONAL WHEEZOMETER
4
Total
4
Cleared
0
Denied
Karmelsonix has 4 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Historical record: 4 cleared submissions from 2007 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Karmelsonix Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Karmelsonix
4 devices