Medical Device Manufacturer · US , Black Diamond , WA

G. Dundas Co.,Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

G. Dundas Co.,Inc. has 2 FDA 510(k) cleared medical devices. Based in Black Diamond, US.

Historical record: 2 cleared submissions from 2008 to 2011. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - G. Dundas Co.,Inc.

2 devices

1-2 of 2