Medical Device Manufacturer · IL , Haifa

Ultraspect , Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2004

Total

Cleared

Denied

Ultraspect , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Haifa, IL.

Historical record: 6 cleared submissions from 2004 to 2011. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Ultraspect , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ultraspect , Ltd.

6 devices

1-6 of 6