FDA 510(k) Applications Submitted by OBERON GMBH FIBER TECHNOLOGIES

FDA 510(k) Number Submission Date Device Name Applicant
K140470 02/25/2014 OBERON: LASER SURGERY FIBER, ATRAUMATIC SURGERY FIBER, SIDE FIRE FIBER, RADIAL EMISSION FIBER, DENTAL SURGERY FIBER OBERON GMBH FIBER TECHNOLOGIES


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