The Siesta Group North America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Siesta Group North America - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
The Siesta Group North America has 1 FDA 510(k) cleared medical devices. Based in Dedham, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by The Siesta Group North America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Siesta Group North America
1 devices