Medical Device Manufacturer · US , Meza , AZ

Intermedic Arfran, SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Intermedic Arfran, SA has 2 FDA 510(k) cleared medical devices. Based in Meza, US.

Historical record: 2 cleared submissions from 2006 to 2009. Primary specialty: General & Plastic Surgery.

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

Intermedic Arfran, SA 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 - Intermedic Arfran, SA

2 devices

1-2 of 2