FDA 510(k) Applications Submitted by PENDRACARE INTERNATIONAL, B.V.

FDA 510(k) Number Submission Date Device Name Applicant
K120585 02/27/2012 CONVEY GUIDING CATHETER PENDRACARE INTERNATIONAL, B.V.
K132197 07/16/2013 CONVEY 7F GUIDING CATHETER, CONVEY 8F GUIDING CATHETER PENDRACARE INTERNATIONAL, B.V.


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