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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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