Medical Device Manufacturer · US , Santa Clara , CA

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

7 submissions · 7 cleared · Since 1988

Total

Cleared

Denied

Cemax, Inc. has 7 FDA 510(k) cleared medical devices. Based in Santa Clara, US.

Historical record: 7 cleared submissions from 1988 to 1995. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Cemax, Inc.

7 devices

1-7 of 7