Biotest-Serum-Institut is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biotest-Serum-Institut - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Biotest-Serum-Institut has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1977 to 1981. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biotest-Serum-Institut Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biotest-Serum-Institut
2 devices