Medical Device Manufacturer · US , Dedham , MA

The Siesta Group North America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Total

Cleared

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

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