FDA 510(k) Applications Submitted by CHRISTINA ROWE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K131437 |
05/20/2013 |
MODIFIED CONCENTRIC MICROCATHETER |
CONCENTRIC MEDICAL, INC. |
| K122478 |
08/14/2012 |
MODIFIED TREVO RETRIEVER |
CONCENTRIC MEDICAL, INC. |
| K122581 |
08/23/2012 |
MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254 |
CONCENTRIC MEDICAL, INC. |
| K003452 |
11/07/2000 |
POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D |
EP TECHNOLOGIES, INC. |
| K021232 |
04/18/2002 |
CONSTELLATION CATHETERS, MODEL 8031M |
BOSTON SCIENTIFIC CORP. |
| K062050 |
07/20/2006 |
FLEXVIEW SYSTEM |
BOSTON SCIENTIFIC |
| K082725 |
09/17/2008 |
GRAFTGUARD PRESSURE CONTROLLING SYRINGE |
MAQUET CARDIOVASCULAR, LLC |
| K034061 |
12/31/2003 |
MODIFICATION TO CONVOY ADVANCED DELIVERY SHEATH |
BOSTON SCIENTIFIC CORP. |
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