Device Classification Name |
wire, guide, catheter
|
510(k) Number |
K131710 |
Device Name |
MERIT HYDROPHILIC GUIDE WIRE |
Applicant |
MERIT MEDICAL SYSTEMS, INC. |
PARKMORE BUSINESS PARK WEST |
GALWAY,
IE
EI
|
|
Applicant Contact |
MARTHA FOLAN |
Correspondent |
MERIT MEDICAL SYSTEMS, INC. |
PARKMORE BUSINESS PARK WEST |
GALWAY,
IE
EI
|
|
Correspondent Contact |
MARTHA FOLAN |
Regulation Number | 870.1330
|
Classification Product Code |
|
Date Received | 06/11/2013 |
Decision Date | 07/29/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|