Medical Device Manufacturer · US , Portland , OR

Atrix - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Atrix Cardiovascular ✕

2 devices

1-2 of 2

Cleared Feb 26, 1986

CARDISUNY 501 A

Cardiovascular · 238d

Cleared Jan 18, 1985

Cardiovascular · 186d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Apr 28, 2026