Esaote is one of 24583 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Esaote has 1 FDA 510(k) cleared medical devices. Based in Carmel, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Esaote Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Esaote
1 devices