FDA 510(k) Applications Submitted by JOHN BALISTRERI

FDA 510(k) Number Submission Date Device Name Applicant
K112044 07/18/2011 ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A ANAXDENT GMBH


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