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FDA 510(k) Applications Submitted by Otto Bock Healthcare Products GmbH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191179
05/02/2019
Myo Plus
Otto Bock Healthcare Products GmbH
K141812
07/07/2014
MYGAIT STIMULATION SYSTEM
OTTO BOCK HEALTHCARE PRODUCTS GMBH
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