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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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