Precise Light Surgical is one of 4785 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precise Light Surgical - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Precise Light Surgical has 1 FDA 510(k) cleared medical devices. Based in Campbell, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Precise Light Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Precise Light Surgical
1 devices