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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