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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