FDA 510(k), K031169, MOTILITY VISUALIZATION SYSTEM

510(K) Number: K031169
Device Name: MOTILITY VISUALIZATION SYSTEM
Manufacturer: SIERRA SCIENTIFIC INSTRUMENTS, INC.
Device Classification Name: System, Gastrointestinal Motility (Electrical)
Regulation Number: 876.1725
Classification Product Code: FFX
Date Received: 04/14/2003
Decision Date: 12/12/2003
Regulation Medical Specialty: Gastroenterology/Urology

152 pages (414 of 566 original pages are fully redacted)