Medical Device Manufacturer · US , Deer Field , IL

Carematix, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2003

Total

Cleared

Denied

Carematix, Inc. has 5 FDA 510(k) cleared medical devices. Based in Deer Field, US.

Historical record: 5 cleared submissions from 2003 to 2012. Primary specialty: Cardiovascular.

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

Carematix, Inc. is one of 5396 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Carematix, Inc. — FDA 510(k) Products and Clearance History

5 devices

1-5 of 5