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FDA 510(k) Applications Submitted by Jamie Howell
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162769
10/03/2016
Pinpoint GT Introducer Needle
C.R. BARD, INC.
K163437
12/07/2016
hypodermic PinpointÖ GT Needle
C. R. Bard, Inc.
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