Aat Alber Antriebstechnik GmbH is one of 19024 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aat Alber Antriebstechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Powered Wheelchair, C-MAX+ (PLUS), C-MAX, C-MAX U1, C-MAX U1 160KG, C-MAX U2, C-MAX U2 160KG, S-MAX, S-MAX AVIATION, S-MAX SELLA, S-MAX SELLA 160KG
3
Total
3
Cleared
0
Denied
Aat Alber Antriebstechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Texas City, US.
Historical record: 3 cleared submissions from 2010 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Aat Alber Antriebstechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beo Medconsulting Berlin GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Aat Alber Antriebstechnik GmbH
3 devices