Kaufmann Sjukvardsartiklar is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kaufmann Sjukvardsartiklar - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kaufmann Sjukvardsartiklar has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kaufmann Sjukvardsartiklar Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kaufmann Sjukvardsartiklar
1 devices