Scopio Labs , Ltd.

Scopio Labs , Ltd. — FDA 510(k) Submissions

Scopio Labs , Ltd. has submitted 4 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Automated Cell-locating, Device, Automated Cell Locating, Bone Marrow . Use the specialty filter in the sidebar to narrow results.