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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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