FDA 510(k) Applications Submitted by PURICORE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K123071 10/01/2012 VASHE SKIN AND WOUND HYDROGEL PURICORE, INC.
K123072 10/01/2012 VASHE WOUND THERAPY SOLUTION PURICORE, INC.
K061689 06/15/2006 AQUATINE EC ENDODONTIC CLEANSER PURICORE, INC.
K063159 10/17/2006 STERILOX LIQUID CHEMICAL STERILANT SYSTEM PURICORE, INC.


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