FDA 510(k) Applications Submitted by CAPSULE TECHNOLOGIE

FDA 510(k) Number Submission Date Device Name Applicant
K020197 01/22/2002 MODIFICATION TO DATACAPTOR CAPSULE TECHNOLOGIE
K032142 07/14/2003 DATACAPTOR CAPSULE TECHNOLOGIE
K013019 09/07/2001 DATACAPTOR CAPSULE TECHNOLOGIE
K180734 03/20/2018 SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie
K183638 12/26/2018 SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie


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