Sandhill Scientific, Inc.

Sandhill Scientific, Inc. — FDA 510(k) Submissions

Sandhill Scientific, Inc. has submitted 16 FDA 510(k) premarket notifications since 1984, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Gastrointestinal Motility (electrical), Electrode, Ph, Stomach, Monitor, Esophageal Motility, Anorectal Motility, And Tube, Cord, Electric, For Endoscope, Stent, Ureteral . Use the specialty filter in the sidebar to narrow results.