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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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