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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