Intratherapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intratherapeutics, Inc. - FDA 510(k) Cleared Devices
15
Total
7
Cleared
0
Denied
Intratherapeutics, Inc. has 7 FDA 510(k) cleared gastroenterology & urology devices. Based in Saint Paul, US.
Historical record: 7 cleared submissions from 1998 to 2001.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intratherapeutics, Inc.
15 devices
Cleared
Aug 13, 2001
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS
Gastroenterology & Urology
117d
Cleared
Jan 24, 2001
INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS
Gastroenterology & Urology
29d
Cleared
Dec 28, 2000
INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY...
Gastroenterology & Urology
90d
Cleared
Dec 07, 2000
INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS
Gastroenterology & Urology
30d
Cleared
Aug 28, 2000
INTRASTENT DOUBLESTRUT PARAMOUNT
Gastroenterology & Urology
90d
Cleared
May 18, 2000
INTRACOIL STENT
General & Plastic Surgery
29d
Cleared
Apr 14, 2000
INTRASTENT DOUBLESTRUT XS STENT
Gastroenterology & Urology
28d
Cleared
Feb 01, 2000
INTRASTENT DOUBLESTRUT LD
Gastroenterology & Urology
76d
Cleared
Oct 15, 1999
MODIFICATION TO INTRASTENT
Gastroenterology & Urology
56d
Cleared
Sep 29, 1999
INTRAMAX ITI GUIDE CATHETER
Cardiovascular
55d
Cleared
Sep 01, 1999
INTRASTENT II
Gastroenterology & Urology
189d
Cleared
Aug 04, 1999
INTRASTENT
Gastroenterology & Urology
57d
Cleared
Jun 02, 1999
INTRACOIL PERIPHERAL STENT
General & Plastic Surgery
131d
Cleared
Apr 07, 1999
ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65
Cardiovascular
370d
Cleared
Jul 21, 1998
ITI STENT
Gastroenterology & Urology
176d