Medical Device Manufacturer · US , Dedham , MA

Curtin & Associates International , Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1997

Total

Cleared

Denied

Curtin & Associates International , Inc. has 0 FDA 510(k) cleared medical devices. Based in Dedham, US.

Historical record: 0 cleared submissions from 1997 to 1997. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Curtin & Associates International , Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Curtin & Associates International , Inc.

1 devices

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