Microlife Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Microlife Corporation has 1 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Microlife Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
1 devices