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FDA 510(k) Applications Submitted by SHELLEY TRIMM
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121085
04/10/2012
HET BIPOLAR LIGATOR SYSTEM
HET SYSTEMS, LLC
K972803
07/28/1997
TRACER O-T-W MAPPING DEVICE
CARDIMA, INC.
K973298
09/02/1997
CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER
CARDIMA, INC.
K122861
09/18/2012
XTOOL
OUROBOROS MEDICAL
K082962
10/03/2008
TIVAMED COOLED RF SYSTEM, MODEL 78001
TIVAMED, INC.
K023922
11/25/2002
COAPT SYSTEMS ENDOTINE DEVICE, MODEL CFD-101-00197
COAPT SYSTEMS, INC.
K974683
12/16/1997
NAVIPORT DEFLECTABLE TIP GUIDING CATHETER
CARDIMA, INC.
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