Applied Imaging Corp.

Applied Imaging Corp. — FDA 510(k) Submissions

Applied Imaging Corp. has submitted 7 FDA 510(k) premarket notifications since 1990, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Automated Scanning Microscope And Image Analysis For Fluorescence In Situ Hybridization (fish) Assays, Device, Automated Cell-locating, Analyzer, Chromosome, Automated, NOT, Microscope, Automated, Image Analysis, Immunohistochemistry,operator Intervention,nuclear Intensity & Percent Positivity . Use the specialty filter in the sidebar to narrow results.