Nano-Ditech Corporation

Nano-Ditech Corporation — FDA 510(k) Submissions

Nano-Ditech Corporation has submitted 6 FDA 510(k) premarket notifications since 2010, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Immunoassay Method, Troponin Subunit, Antigen, Cf (including Cf Controls), Respiratory Syncytial Virus, Multi-analyte Respiratory Virus Antigen Detection Test, Devices Detecting Influenza A, B, And C Virus Antigens, Simple Point-of-care Device To Directly Detect Sars-cov-2 Viral Targets From Clinical Specimens In Near-patient Settings . Use the specialty filter in the sidebar to narrow results.