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FDA 510(k) Applications Submitted by INVATEC S.P.A.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100921
04/02/2010
ADMIRAL XTREME PTA BALLOON DILATATION CATHETER
INVATEC S.P.A.
K092361
08/04/2009
REEF HP 0.035 OTW PTA BALLOON DILATATION CATHETER
INVATEC S.P.A.
K092177
07/21/2009
MO.MA ULTRA PROXIMAL CEREBRAL PROTECTION DEVICE, MODEL MUS0130069X6
INVATEC S.P.A.
K092352
08/04/2009
SCUBA BILIARY STENT SYSTEM
INVATEC S.P.A.
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