FDA 510(k) Applications Submitted by INTRATHERAPEUTICS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K990221 |
01/22/1999 |
INTRACOIL PERIPHERAL STENT |
INTRATHERAPEUTICS, INC. |
K980290 |
01/26/1998 |
ITI STENT |
INTRATHERAPEUTICS, INC. |
K981191 |
04/02/1998 |
ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65 |
INTRATHERAPEUTICS, INC. |
K011184 |
04/18/2001 |
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS |
INTRATHERAPEUTICS, INC. |
K992622 |
08/05/1999 |
INTRAMAX ITI GUIDE CATHETER |
INTRATHERAPEUTICS, INC. |
K003450 |
11/07/2000 |
INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS |
INTRATHERAPEUTICS, INC. |
K003997 |
12/26/2000 |
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS |
INTRATHERAPEUTICS, INC. |
K990592 |
02/24/1999 |
INTRASTENT II |
INTRATHERAPEUTICS, INC. |
K001648 |
05/30/2000 |
INTRASTENT DOUBLESTRUT PARAMOUNT |
INTRATHERAPEUTICS, INC. |
K991929 |
06/08/1999 |
INTRASTENT |
INTRATHERAPEUTICS, INC. |
K992816 |
08/20/1999 |
MODIFICATION TO INTRASTENT |
INTRATHERAPEUTICS, INC. |
K993904 |
11/17/1999 |
INTRASTENT DOUBLESTRUT LD |
INTRATHERAPEUTICS, INC. |
K000864 |
03/17/2000 |
INTRASTENT DOUBLESTRUT XS STENT |
INTRATHERAPEUTICS, INC. |
K001257 |
04/19/2000 |
INTRACOIL STENT |
INTRATHERAPEUTICS, INC. |
K003040 |
09/29/2000 |
INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
INTRATHERAPEUTICS, INC. |
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