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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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