Micro-Bio-Logics

Micro-Bio-Logics — FDA 510(k) Submissions

Micro-Bio-Logics has submitted 9 FDA 510(k) premarket notifications since 1984, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Kit, Quality Control For Culture Media, Culture Media, For Isolation Of Pathogenic Neisseria, Kit, Identification, Enterobacteriaceae, Kit, Identification, Neisseria Gonorrhoeae, Supplement, Culture Media . Use the specialty filter in the sidebar to narrow results.