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FDA 510(k) Applications Submitted by Sonja Toeppen
FDA 510(k) Number
Submission Date
Device Name
Applicant
K183337
12/03/2018
LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2
DMG Chemisch-Pharmazeutische Fabrik GmbH
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