Pat O. Daily is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pat O. Daily - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pat O. Daily has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pat O. Daily Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pat O. Daily
2 devices