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FDA 510(k) Applications Submitted by Robin Haden
FDA 510(k) Number
Submission Date
Device Name
Applicant
K192490
09/11/2019
Tevdek II, Silky II Polydek, 'Cottony' II, NextStitch
Teleflex Medical
K193530
12/20/2019
Deklene MAXX
Teleflex Medical
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