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FDA 510(k) Applications Submitted by MICHELLE R GUDITH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070201
01/22/2007
BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001
C.R. BARD, INC.
K070508
02/22/2007
BARDEX LUBRI-SIL ALL-SILICONE LUBRICIOUS COATED FOLEY CATHETER 6 FR
C.R. BARD, INC.
K073598
12/21/2007
BARD DIGNICARE STOOL MANAGEMENT SYSTEM
C.R. BARD, INC.
K071365
05/15/2007
AGENTO I.C. SILVER-COATED ENDOTRACHEAL TUBE
C.R. BARD, INC.
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