FDA 510(k) Applications Submitted by KARIN GASTINEAU

FDA 510(k) Number Submission Date Device Name Applicant
K051817 07/05/2005 BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEM CARDIVA MEDICAL, INC.
K051827 07/06/2005 JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE JOIMAX GMBH
K123202 10/12/2012 PROCLEAR (OMAFILCON A) SOFT HYDROPHILIC) CONTACT LENS COOPERVISION, INC.
K113759 12/21/2011 AVAIRA (ENFILCON A) CONTACT LENS COOPERVISION, INC.
K080151 01/22/2008 ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039 ANGIOSCORE, INC.


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