Bioview , Ltd.

Bioview , Ltd. — FDA 510(k) Submissions

Bioview , Ltd. has submitted 5 FDA 510(k) premarket notifications since 2003, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Automated Cell-locating, System, Automated Scanning Microscope And Image Analysis For Fluorescence In Situ Hybridization (fish) Assays . Use the specialty filter in the sidebar to narrow results.