Denka Seiken'S is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Denka Seiken'S - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Denka Seiken'S has 4 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Historical record: 4 cleared submissions from 1998 to 2002. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Denka Seiken'S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Denka Seiken'S
4 devices