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FDA 510(k) Applications Submitted by Katalyst Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171035
04/06/2017
Katalyst Mark 1 Muscle Stimulation System
Katalyst Inc.
K190966
04/12/2019
Katalyst Training System
Katalyst Inc.
K181199
05/07/2018
Katalyst Mark 1 Muscle Stimulation System Model 2
Katalyst Inc.
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