Medical Device Manufacturer · US , Research Triangle , NC

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

4 submissions · 4 cleared · Since 1984

Total

Cleared

Denied

Glaxo, Inc. has 4 FDA 510(k) cleared medical devices. Based in Research Triangle, US.

Historical record: 4 cleared submissions from 1984 to 1995. Primary specialty: General Hospital.

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

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

4 devices

1-4 of 4