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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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