Device Classification Name |
System, Catheter Control, Steerable
|
510(k) Number |
K090365 |
Device Name |
HANSEN MEDICAL ARTISAN S CONTROL CATHETER |
Applicant |
HANSEN MEDICAL, INC. |
800 E. MIDDLEFIELD ROAD |
MOUNTAIN VIEW,
CA
94043
|
|
Applicant Contact |
KATE WHITIN |
Correspondent |
HANSEN MEDICAL, INC. |
800 E. MIDDLEFIELD ROAD |
MOUNTAIN VIEW,
CA
94043
|
|
Correspondent Contact |
KATE WHITIN |
Regulation Number | 870.1290
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 02/13/2009 |
Decision Date | 05/07/2009 |
Decision |
SE - With Limitations
(SESU) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|