Medical Device Manufacturer · US , Blain , WA

Garaventa Accessibility - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Garaventa Accessibility has 2 FDA 510(k) cleared medical devices. Based in Blain, US.

Historical record: 2 cleared submissions from 2002 to 2004. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Garaventa Accessibility Filter by specialty or product code using the sidebar.

Garaventa Accessibility is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Garaventa Accessibility

2 devices

1-2 of 2