FDA 510(k) Applications Submitted by EST. ANTHOGYR

FDA 510(k) Number Submission Date Device Name Applicant
K020431 02/08/2002 FIBIOCORE EST. ANTHOGYR
K070084 01/09/2007 MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL EST. ANTHOGYR
K060317 02/08/2006 ANTHOGYR CONTRA ANGLES AND HANDPIECES EST. ANTHOGYR


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