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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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