FDA 510(k) Applications Submitted by FLEXICATH LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K063363 11/07/2006 FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE FLEXICATH LTD.
K080793 03/20/2008 FIRMGRIP FLEXICATH LTD.
K111939 07/08/2011 M/29TM - PRESSURE INJECTABLE FLEXICATH LTD.
K092629 08/27/2009 SNM FIRMGRIP FLEXICATH LTD.


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