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FDA 510(k) Applications Submitted by JACOB LEE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170158
01/18/2017
PowerGlide ST Midline Catheter
C. R. Bard, Inc.
K191976
07/24/2019
Piper GO-IO Intraosseous Infusion System
Piper Access, LLC
K162377
08/24/2016
PowerGlide Pro Midline Catheter
C.R. BARD, INC.
K223088
09/30/2022
BD SmartSiteÖ Needle-Free Connector
CareFusion
K162894
10/17/2016
AccuCath Intravascular Catheter
C.R.BARD, INC.
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