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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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