Motilitycount Aps

Motilitycount Aps — FDA 510(k) Submissions

Motilitycount Aps has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Semen Analysis Device, Labware, Assisted Reproduction . Use the specialty filter in the sidebar to narrow results.