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FDA 510(k) Applications Submitted by EVALVE INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091596
06/02/2009
EVALVE STEERABLE GUIDE CATHETER, MODEL SGC01ST
EVALVE INC
K100789
03/22/2010
MODIFICATON TO: STEERABLE GUIDE CATHETER, MODEL SGC01ST
EVALVE INC
K083793
12/22/2008
STEERABLE GUIDE CATHETER
EVALVE INC
K093866
12/17/2009
EVALVE STEERABLE GUIDE CATHETER
EVALVE INC
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