Livemetric (Medical) S.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Livemetric (Medical) S.A. has 1 FDA 510(k) cleared medical devices. Based in Luxemburg, LU.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Livemetric (Medical) S.A. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Livemetric (Medical) S.A.
1 devices