Medical Device Manufacturer · US , Beaverton , OR

Extension , Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2013

Official Website

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Extension , Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Jul 11, 2013

CLINICAL ALERT NOTIFICATION

Cardiovascular · 150d