Lifecare , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Lifecare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LIVIA
3
Total
3
Cleared
0
Denied
Lifecare , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.
Historical record: 3 cleared submissions from 2001 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Lifecare , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cohen, Tauber, Spievack & Wagner as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Lifecare , Ltd.
3 devices