Medical Device Manufacturer · US , Boulder , CO

H&O Equipments, Nv/Sa - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

H&O Equipments, Nv/Sa has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.

Historical record: 2 cleared submissions from 2003 to 2016. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by H&O Equipments, Nv/Sa Filter by specialty or product code using the sidebar.

H&O Equipments, Nv/Sa is one of 4767 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - H&O Equipments, Nv/Sa

2 devices

1-2 of 2