FDA 510(k) Applications Submitted by Michele Davis

FDA 510(k) Number Submission Date Device Name Applicant
K150699 03/18/2015 Bard LubriGuard Foley Catheter C.R. Bard, Inc.
K140856 04/03/2014 BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS C.R. BARD, INC.
K142575 09/12/2014 Bard RiteCath Intermittent Urinary Catheter C.R. Bard, Inc.
K123179 10/09/2012 AJUST HELICAL ADJUSTABLE SINGLE-INCISION SLING C.R. BARD, INC.
K133251 10/22/2013 BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM C.R. BARD, INC.
K133470 11/12/2013 BARD RITECATH INTERMITTENT CATHETER C.R. BARD, INC.


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