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FDA 510(k) Applications Submitted by Storz Medical AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K202112
07/30/2020
Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece
Storz Medical AG
K173692
12/01/2017
D-Actor 200 Vibration Massage System
Storz Medical AG
K203710
12/21/2020
Storz Medical MAGNETOLITH Muscle Stimulator
Storz Medical AG
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