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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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