FDA 510(k) Applications Submitted by SUZANNE SCHORLE

FDA 510(k) Number Submission Date Device Name Applicant
K111117 04/21/2011 CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC... Teleflex Medical, Inc.
K041740 06/28/2004 SILICONE COATED GUIDEWIRE ARROW INTERNATIONAL, INC.
K111900 07/05/2011 NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER Teleflex Medical, Inc.
K042126 08/06/2004 PICC ARROW INTL., INC.
K102238 08/09/2010 ARROW(R) NEXTSTEP TM ANTEGRADE CHRONIC HEMODIALYSIS CATHETER Teleflex Medical, Inc.


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