FDA 510(k) Applications Submitted by JUMA HOSHINO

FDA 510(k) Number Submission Date Device Name Applicant
K141311 05/20/2014 0.9% SODIUM CHLORIDE INJECTION, USP BD POSIFLUSH; SP SYRINGE, SF SYRINGE Becton, Dickinson and Company
K113409 11/18/2011 S2 FEMORAL A/R NAIL S2 FEMORAL COMRESSION NAIL S2 TIBIAL NAIL S2 TIBIAL COMPRESSION NAIL HOWMEDICA OSTEONICS CORP.
K193356 12/04/2019 BiZact Tonsillectomy Device Advanced Bipolar Tissue Sealer/Divider Covidien, LLC


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