Louise C. Myers is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Louise C. Myers - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Louise C. Myers has 1 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Louise C. Myers Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Louise C. Myers
1 devices