Device Classification Name |
introducer, catheter
|
510(k) Number |
K870374 |
Device Name |
PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK |
Applicant |
DAIG CORP. |
14901 DEVEAU PLACE |
MINNETONKA,
MN
55345 -2126
|
|
Applicant Contact |
JOHN FLEISCHHACKER |
Correspondent |
DAIG CORP. |
14901 DEVEAU PLACE |
MINNETONKA,
MN
55345 -2126
|
|
Correspondent Contact |
JOHN FLEISCHHACKER |
Regulation Number | 870.1340
|
Classification Product Code |
|
Date Received | 01/29/1987 |
Decision Date | 03/18/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|