Medical Device Manufacturer · US , Washington , DC

Lifetrac, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

Total

Cleared

Denied

Lifetrac, Inc. has 1 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Lifetrac, Inc.

1 devices

1-1 of 1