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

Substantially Equivalent

Clinical Innovations, Inc.

FDA 510(k) clearance K022023 for COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500, Substantially Equivalent on 2003-01-07. Applicant: Clinical Innovations, Inc..

Clearance details

Applicant: Clinical Innovations, Inc.
Product code: Code KLA
Advisory panel: Gastroenterology, Urology
Date received: 2002-06-20
Decision date: 2003-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murray, UT, US

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