Medical Device Manufacturer · DE , Tuttlingen

Henke-Sass, Wolf GmbH - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Henke-Sass, Wolf GmbH has 6 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.

Historical record: 6 cleared submissions from 1994 to 2018.

Browse the FDA 510(k) cleared devices submitted by Henke-Sass, Wolf GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Henke-Sass, Wolf GmbH

6 devices

1-6 of 6