FDA 510(k) Applications Submitted by SKIP RIMER

FDA 510(k) Number Submission Date Device Name Applicant
K080170 01/24/2008 AGENTO I.C. SILVER-COATED ENDOTRACHEAL TUBE (IHVLP) C.R. BARD, INC.
K120234 01/25/2012 EZONO 3000 LIFE-TECH, INC.
K070558 02/27/2007 BARDEX LUBRI-SIL AND BARDEX LUBRI-SIL I.C. ANTI-INFECTIVE ALL-SILICONE FOLEY CATHETERS C.R. BARD, INC.
K070582 03/01/2007 BARDEX ALL-SILICONE, BARDEX LUBRI-SIL, AND BARDEX LUBRI-SIL I.C. TEMPERATURE-SENSING FOLEY CATHETERS C.R. BARD, INC.
K111355 05/16/2011 ECHOBRIGHT LIFE-TECH, INC.
K102813 09/28/2010 EZONO 3000 LIFE-TECH, INC.


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