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FDA 510(k), K031169, MOTILITY VISUALIZATION SYSTEM
FDA 510(k), K031169, MOTILITY VISUALIZATION SYSTEM
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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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