Dr. August Wolff GmbH & Co. KG Arzeimittel is one of 199 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dr. August Wolff GmbH & Co. KG Arzeimittel - FDA 510(k) Cleared Devic...
1
Total
1
Cleared
0
Denied
Dr. August Wolff GmbH & Co. KG Arzeimittel has 1 FDA 510(k) cleared medical devices. Based in Bielefeld, DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Dr. August Wolff GmbH & Co. KG Arzeimittel Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dr. August Wolff GmbH & Co. KG Arzeimittel
1 devices