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Intratherapeutics, Inc.

15 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS (K011184)Intratherapeutics, Inc.2001-08-13
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS (K003997)Intratherapeutics, Inc.2001-01-24
INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY (K003040)Intratherapeutics, Inc.2000-12-28
INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS (K003450)Intratherapeutics, Inc.2000-12-07
INTRASTENT DOUBLESTRUT PARAMOUNT (K001648)Intratherapeutics, Inc.2000-08-28
INTRACOIL STENT (K001257)Intratherapeutics, Inc.2000-05-18
INTRASTENT DOUBLESTRUT XS STENT (K000864)Intratherapeutics, Inc.2000-04-14
INTRASTENT DOUBLESTRUT LD (K993904)Intratherapeutics, Inc.2000-02-01
MODIFICATION TO INTRASTENT (K992816)Intratherapeutics, Inc.1999-10-15
INTRAMAX ITI GUIDE CATHETER (K992622)Intratherapeutics, Inc.1999-09-29
INTRASTENT II (K990592)Intratherapeutics, Inc.1999-09-01
INTRASTENT (K991929)Intratherapeutics, Inc.1999-08-04
INTRACOIL PERIPHERAL STENT (K990221)Intratherapeutics, Inc.1999-06-02
ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65 (K981191)Intratherapeutics, Inc.1999-04-07
ITI STENT (K980290)Intratherapeutics, Inc.1998-07-21

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Every clearance here is in the API, with alerts when new ones post.