Bionetic Laboratory Products

Bionetic Laboratory Products — FDA 510(k) Submissions

Bionetic Laboratory Products has submitted 8 FDA 510(k) premarket notifications since 1983, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Bath, Incubators/water, All, Reagents, Antibody, Legionella, Direct & Indirect Fluorescent, Antigens, If, Toxoplasma Gondii, Enzyme Linked Immunoabsorbent Assay, Varicella-zoster, Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp. . Use the specialty filter in the sidebar to narrow results.