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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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