FDA 510(k) Applications Submitted by Laura Moen-Ftacek

FDA 510(k) Number Submission Date Device Name Applicant
K070417 02/12/2007 ACROSS TRANSSEPTAL ACCESS SYSTEM, 406977, 406978, 406979, 406980, 406981, 406982, 406983, 406984 ST. JUDE MEDICAL
K141858 07/10/2014 CLOSURERFG RADIOFREQUENCY GENERATOR COVIDIEN
K072012 07/23/2007 REFLEXION SPIRAL VARIABLE RADIUS CATHETER ST. JUDE MEDICAL
K072278 08/16/2007 BRK TRANSSEPTAL NEEDLE ST. JUDE MEDICAL
K083083 10/16/2008 AGILIS NXT STEERABLE INTRODUCER ST. JUDE MEDICAL
K103083 10/19/2010 AGILIS ES STEERABLE INTRODUCER ST. JUDE MEDICAL


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