Medical Device Manufacturer · US , Santa Ana , CA

Newport Biosystems, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

Total

Cleared

Denied

Newport Biosystems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Santa Ana, US.

Historical record: 4 cleared submissions from 1985 to 1988. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Newport Biosystems, Inc.

4 devices

1-4 of 4