Dragerwerk AG & CO Kgaa is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dragerwerk AG & CO Kgaa - FDA 510(k) Cleared Devices
Recent clearances: Babyleo TN500, Savina 300
2
Total
2
Cleared
0
Denied
Dragerwerk AG & CO Kgaa has 2 FDA 510(k) cleared medical devices. Based in L?beck, DE.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dragerwerk AG & CO Kgaa Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Draeger Medical Sytems, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dragerwerk AG & CO Kgaa
2 devices