FDA 510(k), K881609, SITZMARKS

FDA 510(k), K881609, SITZMARKS

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510(K) Number: K881609
Device Name: SITZMARKS
Manufacturer:
Device Classification Name: System, Gastrointestinal Motility (Electrical)
Regulation Number: 876.1725
Classification Product Code: FFX
Date Received: 04/12/1988
Decision Date: 07/08/1988
Regulation Medical Specialty: Gastroenterology/Urology
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