Medical Device Manufacturer · US , Stewartville , MN

Arcon Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1984

Total

Cleared

Denied

Arcon Corp. has 2 FDA 510(k) cleared medical devices. Based in Stewartville, US.

Historical record: 2 cleared submissions from 1984 to 1988. Primary specialty: Obstetrics & Gynecology.

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

Arcon Corp. 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 - Arcon Corp.

2 devices

1-2 of 2