FDA 510(k), K022023, COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

FDA 510(k), K022023, COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

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510(K) Number: K022023
Device Name: COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500
Manufacturer: CLINICAL INNOVATIONS, INC.
Device Classification Name: Monitor, Esophageal Motility, Anorectal Motility, And Tube
Regulation Number: 876.1725
Classification Product Code: KLA
Date Received: 06/20/2002
Decision Date: 01/07/2003
Regulation Medical Specialty: Gastroenterology/Urology

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