FDA 510(k) Applications Submitted by SCHOLLY FIBEROPTIC GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K984556 12/23/1998 SCICAN CLASSIC SCHOLLY FIBEROPTIC GMBH
K133682 12/02/2013 SCHOELLY ARTHROSCOPE SCHOLLY FIBEROPTIC GMBH
K141366 05/23/2014 VIDEO BRONCHOSCOPE SYSTEM SCHOLLY FIBEROPTIC GMBH


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