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FDA 510(k) Applications Submitted by William Heard
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150345
02/11/2015
Magic3 Go Intermittent Urinary Catheter
C.R. BARD, INC.
K161581
06/08/2016
Arthrex Synergy RF System
ARTHREX, INC.
K091761
06/16/2009
TELEFLEX ISIS HVT TRACHEAL TUBE, CUFFED, WITH SUBGLOTTIC SECRETION SUCTION PORT
Teleflex Medical, Inc.
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