Oismuller & Partner Keg is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Oismuller & Partner Keg - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Oismuller & Partner Keg has 0 FDA 510(k) cleared medical devices. Based in Austria, AT.
Historical record: 0 cleared submissions from 1995 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Oismuller & Partner Keg Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oismuller & Partner Keg
1 devices