FDA 510(k) Applications Submitted by MARIA BRITTLE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K961499 |
04/18/1996 |
LAGUNA SOFTIP DIAGNOSTIC CATHETERS |
BOSTON SCIENTIFIC SCIMED, INC. |
| K981413 |
04/20/1998 |
SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS |
BOSTON SCIENTIFIC SCIMED, INC. |
| K961999 |
05/22/1996 |
SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS |
BOSTON SCIENTIFIC SCIMED, INC. |
| K040653 |
03/12/2004 |
PARAMOUNT MINI GPS BILIARY STENT SYSTEM |
EV3 INC |
| K000864 |
03/17/2000 |
INTRASTENT DOUBLESTRUT XS STENT |
INTRATHERAPEUTICS, INC. |
| K080901 |
03/31/2008 |
LBI EMBOLECTOMY SYSTEM |
LUMEN BIOMEDICAL, INC. |
| K001257 |
04/19/2000 |
INTRACOIL STENT |
INTRATHERAPEUTICS, INC. |
| K021563 |
05/13/2002 |
INTRACOIL SELF-EXPANDING PERIPHERAL STENT |
SULZER INTRATHERAPEUTICS, INC. |
| K021729 |
05/24/2002 |
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
SULZER INTRATHERAPEUTICS, INC. |
| K071529 |
06/05/2007 |
XTRACT CATHETER SYSTEM |
LUMEN BIOMEDICAL, INC. |
| K011806 |
06/11/2001 |
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
SULZER INTRATHERAPEUTICS, INC. |
| K012066 |
07/02/2001 |
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
SULZER INTRATHERAPEUTICS, INC. |
| K082348 |
08/15/2008 |
FIBERNET EMBOLIC PROTECTION SYSTEM |
LUMEN BIOMEDICAL, INC. |
| K003040 |
09/29/2000 |
INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
INTRATHERAPEUTICS, INC. |
| K023243 |
09/30/2002 |
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
SULZER INTRATHERAPEUTICS, INC. |
| K014136 |
12/17/2001 |
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY |
SULZER INTRATHERAPEUTICS, INC. |
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