Lifesignals, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Lifesignals, Inc. has 3 FDA 510(k) cleared medical devices. Based in Fremont, US.
Latest FDA clearance: Nov 2024. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lifesignals, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.
3 devices