Draeget Medical AG & Co. Kgaa is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Draeget Medical AG & Co. Kgaa - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Draeget Medical AG & Co. Kgaa has 2 FDA 510(k) cleared medical devices. Based in Telford, US.
Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Draeget Medical AG & Co. Kgaa Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Draeget Medical AG & Co. Kgaa
2 devices