Medical Device Manufacturer · US , Glendale , WI

Etac Us, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Etac Us, Inc. has 5 FDA 510(k) cleared medical devices. Based in Glendale, US.

Historical record: 5 cleared submissions from 1988 to 1993. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Etac Us, Inc. Filter by specialty or product code using the sidebar.

Etac Us, Inc. 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 - Etac Us, Inc.

5 devices

1-5 of 5