Device Classification Name |
catheter, intravascular, diagnostic
|
510(k) Number |
K932420 |
Device Name |
SCIMED 6 FR., 7 FR., AND 8 FR.,TRIGUIDE GUIDING |
Applicant |
SCIMED LIFE SYSTEMS, INC. |
6655 WEDGWOOD RD. |
MAPLE GROVE,
MN
55311 -3616
|
|
Applicant Contact |
DAVID A TEICHER |
Correspondent |
SCIMED LIFE SYSTEMS, INC. |
6655 WEDGWOOD RD. |
MAPLE GROVE,
MN
55311 -3616
|
|
Correspondent Contact |
DAVID A TEICHER |
Regulation Number | 870.1200
|
Classification Product Code |
|
Date Received | 05/19/1993 |
Decision Date | 08/17/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|