FDA 510(k) Applications Submitted by BRIAN D FARIAS

FDA 510(k) Number Submission Date Device Name Applicant
K160235 02/01/2016 ViaValve Safety I.V. Catheter SMITHS MEDICAL ASD, INC.
K061194 04/28/2006 PORTEX NEEDLE-PRO EDGE SAFETY WITH SYRINGE, MODELS 432310, 432210, 432510, 432558 SMITHS MEDICAL ASD, INC.
K081229 04/30/2008 SAF-T CLOSED BLOOD COLLECTION SYSTEM WITH SAF-HOLDER DEVICE, WITH 21G, 23G, 25G SAF-T WING SMITHS MEDICAL ASD, INC.
K071785 07/02/2007 HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE, HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE WITH SYRINGE SMITHS MEDICAL ASD, INC.
K072482 09/04/2007 HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY SMITHS MEDICAL ASD, INC.
K072783 10/01/2007 SAF-T CLOSED BLOOD COLLECTION SYSTEM WITH SAF-HOLDER DEVICE, MODEL 99200, SAF-T CLOSED BLOOD COLLECTION SYSTEM WITH SMITHS MEDICAL ASD, INC.
K073188 11/13/2007 HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE SMITHS MEDICAL ASD, INC.
K063450 11/15/2006 PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110 SMITHS MEDICAL ASD, INC.
K113700 12/16/2011 VIAVALVE SAFETY IV CATHETER SMITHS MEDICAL ASD, INC.
K063755 12/19/2006 PORTEX HYPODERMIC NEEDLE-PRO FIXED NEEDLE SYRINGE SMITHS MEDICAL ASD, INC.
K001318 04/26/2000 CPAP SYSTEM, MODEL 102001 SIMS PORTEX, INC.
K041399 05/26/2004 HYPODERMIC NEEDLE-PRO EDGE NEEDLE PROTECTION DEVICE SMITHS MEDICAL ASD, INC.


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