Device Classification Name |
Catheter, Percutaneous
|
510(k) Number |
K092298 |
Device Name |
MODIFICATION TO MODIFIED HD GUIDE CATHETER |
Applicant |
CONCENTRIC MEDICAL, INC. |
301 E. EVELYN AVE. |
MOUNTAIN VIEW,
CA
94041
|
|
Applicant Contact |
KIRSTEN VALLEY |
Correspondent |
CONCENTRIC MEDICAL, INC. |
301 E. EVELYN AVE. |
MOUNTAIN VIEW,
CA
94041
|
|
Correspondent Contact |
KIRSTEN VALLEY |
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 07/29/2009 |
Decision Date | 11/05/2009 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|