Medspira, LLC

Medspira, LLC — FDA 510(k) Submissions

Medspira, LLC has submitted 3 FDA 510(k) premarket notifications since 2012, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Esophageal Motility, Anorectal Motility, And Tube, System, Gastrointestinal Motility (electrical) . Use the specialty filter in the sidebar to narrow results.