Medical Device Manufacturer · US , Columbus , OH

Ross Product Div. Abbott Laboratories - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1999

Total

Cleared

Denied

Ross Product Div. Abbott Laboratories has 4 FDA 510(k) cleared medical devices. Based in Columbus, US.

Historical record: 4 cleared submissions from 1999 to 2003. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Ross Product Div. Abbott Laboratories Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ross Product Div. Abbott Laboratories

4 devices

1-4 of 4