Device Classification Name |
catheter, intravascular, therapeutic, short-term less than 30 days
|
510(k) Number |
K850349 |
Device Name |
VIGGO ARTERIAL CANNULA |
Applicant |
VIGGO PRODUCTS |
OHMEDA |
P.O. BOX 7550 |
MADISON,
WI
53707
|
|
Applicant Contact |
RAYMOND T RIDDLE |
Correspondent |
VIGGO PRODUCTS |
OHMEDA |
P.O. BOX 7550 |
MADISON,
WI
53707
|
|
Correspondent Contact |
RAYMOND T RIDDLE |
Regulation Number | 880.5200
|
Classification Product Code |
|
Date Received | 01/28/1985 |
Decision Date | 04/09/1985 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|