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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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