Device Classification Name |
catheter, percutaneous
|
510(k) Number |
K940603 |
Device Name |
SCIMED 8 FRENCH TRIGUIDE GUIDING CATHETER |
Applicant |
SCIMED LIFE SYSTEMS, INC. |
2050 EAST CENTER CIRCLE |
PLYMOUTH,
MN
55441
|
|
Applicant Contact |
DIANE M LOWE |
Correspondent |
SCIMED LIFE SYSTEMS, INC. |
2050 EAST CENTER CIRCLE |
PLYMOUTH,
MN
55441
|
|
Correspondent Contact |
DIANE M LOWE |
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 02/09/1994 |
Decision Date | 04/19/1994 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|