FDA 510(k) Applications Submitted by JENNIFER RUETHER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100093 |
01/13/2010 |
VSI TORQUE DEVICE |
VASCULAR SOLUTIONS, INC. |
| K061282 |
05/08/2006 |
ACCESS ULTRASENSITIVE HGH CALIBRATOR, MODEL 33585 |
BECKMAN COULTER, INC. |
| K111334 |
05/12/2011 |
BENELLI ACCESS DEVICE |
VASCULAR SOLUTIONS, INC. |
| K101604 |
06/08/2010 |
VSI MICRO-INTRODUCER SETS (REGULAR, STIFFEN), MODELS 7197V-7209V, 7240V-7256V, 7259V, 7230V, 7231V, 7260V, 7274V |
VASCULAR SOLUTIONS, INC. |
| K101625 |
06/09/2010 |
COHEN CROSSOVER CATHETER |
VASCULAR SOLUTIONS, INC. |
| K122301 |
08/01/2012 |
GUARDIAN II HEMOSTASIS VALVE GUARDIAN II NC HEMOSTASIS VALVE |
VASCULAR SOLUTIONS ZERUSA LTD. |
| K172393 |
08/08/2017 |
Advisor HD Grid Mapping Catheter, Sensor Enabled |
St. Jude Medical, Inc. |
| K113266 |
11/04/2011 |
GEL-BLOCK EMBOLIZATION PLEDGETS |
VASCULAR SOLUTIONS, INC. |
| K093502 |
11/12/2009 |
VARI-LASE ENDOVENOUS LASER CONSOLE |
VASCULAR SOLUTIONS, INC. |
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