FDA 510(k) Applications Submitted by BRIAN 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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