Medical Device Manufacturer · US , Crofton , MD

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

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Lifelines , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 4 cleared submissions from 2001 to 2018. Primary specialty: Neurology.

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

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

4 devices

1-4 of 4