FDA 510(k) Applications Submitted by JOAN Q BARTLE

FDA 510(k) Number Submission Date Device Name Applicant
K100351 02/12/2010 NEUROSCOUT STEERABLE GUIDEWIRE Codman & Shurtleff, Inc.
K121776 06/18/2012 AGILITY STEERABLE GUIDEWIRE NEUROSCOUT STEERABLE GUDIEWIRE Codman & Shurtleff, Inc.
K052449 09/06/2005 CADMAN INTEGRATED IRRIGATION TUBING AND BIPOLAR CORD SET, MODELS 80-1163, 80-1189 Codman & Shurtleff, Inc.


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