Medical Device Manufacturer · US , Brookline , MA

Core-M, Inc. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Core-M, Inc. has 2 FDA 510(k) cleared medical devices. Based in Brookline, US.

Historical record: 2 cleared submissions from 1989 to 1996. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Core-M, Inc. Filter by specialty or product code using the sidebar.

Core-M, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Core-M, Inc.

3 devices

1-3 of 3