Laborie Medical Technologies, Corp.

Laborie Medical Technologies, Corp. — FDA 510(k) Submissions

Laborie Medical Technologies, Corp. has submitted 5 FDA 510(k) premarket notifications since 2008, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Cystometric, Hydraulic, System, Imaging, Pulsed Echo, Ultrasonic, Monitor, Esophageal Motility, Anorectal Motility, And Tube, System, Gastrointestinal Motility (electrical), Endoscopic Injection Needle, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.