Intratherapeutics, Inc.
Intratherapeutics, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2001.
Top product codes for Intratherapeutics, Inc.
Recent clearances by Intratherapeutics, Inc.
- K011184 — INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS
- K003997 — INTRASTENT DOUBLESTRUT PARAMOUNT XS BILIARY ENDOPROSTHESIS
- K003040 — INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
- K003450 — INTRASTENT DOUBLESTRUT PARAMOUNT BILIARY ENDOPROSTHESIS
- K001648 — INTRASTENT DOUBLESTRUT PARAMOUNT
- K001257 — INTRACOIL STENT
- K000864 — INTRASTENT DOUBLESTRUT XS STENT
- K993904 — INTRASTENT DOUBLESTRUT LD
- K992816 — MODIFICATION TO INTRASTENT
- K992622 — INTRAMAX ITI GUIDE CATHETER
- K990592 — INTRASTENT II
- K991929 — INTRASTENT
- K990221 — INTRACOIL PERIPHERAL STENT
- K981191 — ITI INTRAMAX GUIDE CATHETER 91, 78 AND 65
- K980290 — ITI STENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.