FDA 510(k) Applications Submitted by JAMES WILKIE

FDA 510(k) Number Submission Date Device Name Applicant
K090270 02/04/2009 BACKSTOP CATHETER, MODEL 60-0000-3100 PLUROMED, INC.
K090430 02/19/2009 BACKSTOP AND BACKSTOP INJECTOR PLUROMED, INC.
K110491 02/22/2011 BACKSTOP CATHETER PLUROMED, INC.
K103349 11/16/2010 BACKSTOP CATHETER PLUROMED, INC.


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