FDA 510(k) Applications Submitted by DIANE CARROLL

FDA 510(k) Number Submission Date Device Name Applicant
K091793 06/17/2009 AMPLATZER TORQVUE 3 DELIVERY SHEATH, MODEL 9-TV3-08F104, 9-TV3-08F54 AGA MEDICAL CORP.
K083214 10/31/2008 AMPLATZER TORQVUE 45DEGREEX45DEGREE DELIVERY SHEATH, MODELS 9-TV45X45-09F-100, 9-TV45X45-10F-100 AGA MEDICAL CORP.


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