FDA 510(k) Applications Submitted by CHRISTOPHER WATKINS

FDA 510(k) Number Submission Date Device Name Applicant
K140473 02/25/2014 DUALGUARD FLEXICARE MEDICAL LTD.
K132619 08/21/2013 CLASSIC INTERMITTENT CATHETER FLEXICARE MEDICAL LTD.
K133516 11/15/2013 CO2 MONITORING LINE, CO2 MONITORING LINE WITH FILTER FLEXICARE


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