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Intratherapeutics, Inc.

FDA 510(k) & PMA Approved Devices — 15 products

Total Devices15
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K011184 INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESISFGE2001-08-13 View
510(k) K003997 INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESISFGE2001-01-24 View
510(k) K003040 INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGYFGE2000-12-28 View
510(k) K003450 INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESISFGE2000-12-07 View
510(k) K001648 INTRASTENT DOUBLESTRUT PARAMOUNTFGE2000-08-28 View
510(k) K001257 INTRACOIL STENTJCT2000-05-18 View
510(k) K000864 INTRASTENT DOUBLESTRUT XS STENTFGE2000-04-14 View
510(k) K993904 INTRASTENT DOUBLESTRUT LDFGE2000-02-01 View
510(k) K992816 MODIFICATION TO INTRASTENTFGE1999-10-15 View
510(k) K992622 INTRAMAX ITI GUIDE CATHETERDQY1999-09-29 View
510(k) K990592 INTRASTENT IIFGE1999-09-01 View
510(k) K991929 INTRASTENTFGE1999-08-04 View
510(k) K990221 INTRACOIL PERIPHERAL STENTJCT1999-06-02 View
510(k) K981191 ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65DQY1999-04-07 View
510(k) K980290 ITI STENTFGE1998-07-21 View
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