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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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