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FDA 510(k) Applications Submitted by INTERVALVE, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K123111
10/03/2012
V8 TRANSLUMINAL BAV CATHETER
INTERVALVE, INC
K133607
11/25/2013
V8 TRANSLUMINAL BAV CATHETER
INTERVALVE, INC
K132728
09/03/2013
V8 TRANSLUMINAL BAV CATHETER
INTERVALVE, INC
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