Lifelines , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lifelines , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Trackit T4 EEG Amplifier
4
Total
4
Cleared
0
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.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Lifelines , Ltd.
4 devices