Ps Advanced Engineering is one of 5631 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ps Advanced Engineering - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ps Advanced Engineering has 2 FDA 510(k) cleared medical devices. Based in Alhambra, US.
Historical record: 2 cleared submissions from 2010 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ps Advanced Engineering Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ps Advanced Engineering
2 devices