Cetro America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cetro America - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Cetro America has 1 FDA 510(k) cleared medical devices. Based in Hamden, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Cetro America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cetro America
1 devices