Medical Device Manufacturer · IL , Binyamina

Karmelsonix - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2007

Total

Cleared

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

1-4 of 4