Device Classification Name |
Catheter, Percutaneous
|
510(k) Number |
K950094 |
Device Name |
SCIMED 6 FRENCH MICRO-MAX(TM) GUIDE CATHETER |
Applicant |
SCIMED LIFE SYSTEMS, INC. |
8200 SCIMED PLACE |
MAPLE GROVE,
MN
55311 -1566
|
|
Applicant Contact |
DIANE M LOWE |
Correspondent |
SCIMED LIFE SYSTEMS, INC. |
8200 SCIMED PLACE |
MAPLE GROVE,
MN
55311 -1566
|
|
Correspondent Contact |
DIANE M LOWE |
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 01/10/1995 |
Decision Date | 03/03/1995 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|