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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