ROTA-DAN RAPID ROTAVIRUS EIA KIT
Feb 1996
334d
Eldan Technologies, Ltd.
1
Total
1
Cleared
0
Denied
Eldan Technologies, Ltd. — FDA 510(k) Submissions
Eldan Technologies, Ltd. has submitted 1 FDA 510(k) premarket notifications since 1996, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Enzyme Linked Immunoabsorbent Assay, Rotavirus . Use the specialty filter in the sidebar to narrow results.
1 devices