Liv International USA, Inc. is one of 23674 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Liv International USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIV BREAST SELF EXAMINATION AID
1
Total
1
Cleared
0
Denied
Liv International USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Liv International USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Liv International USA, Inc.
1 devices