POCKIT HSV 2 RAPID TEST
Aug 1999
290d
Diagnology , Ltd.
1
Total
1
Cleared
0
Denied
Diagnology , Ltd. — FDA 510(k) Submissions
Diagnology , Ltd. has submitted 1 FDA 510(k) premarket notifications since 1999, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-specific . Use the specialty filter in the sidebar to narrow results.
1 devices