Acon Laboratories Co.

Acon Laboratories Co. — FDA 510(k) Submissions

Acon Laboratories Co. has submitted 6 FDA 510(k) premarket notifications since 1998, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antigens, All Groups, Streptococcus Spp., Enzyme Immunoassay, Amphetamine, Diazonium Colorimetry, Urobilinogen (urinary, Non-quant.), System, Test, Blood Glucose, Over The Counter, Visual, Pregnancy Hcg, Prescription Use . Use the specialty filter in the sidebar to narrow results.