Dwl Elektronische Systeme GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dwl Elektronische Systeme GmbH - FDA 510(k) Cleared Devices
Recent clearances: HEMO-DOP
1
Total
1
Cleared
0
Denied
Dwl Elektronische Systeme GmbH has 1 FDA 510(k) cleared medical devices. Based in Sipplingen, DE.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dwl Elektronische Systeme GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dwl Elektronische Systeme GmbH
1 devices