Device Classification Name |
Dialyzer, Single Coil
|
510(k) Number |
K760702 |
Device Name |
ERI-FLO 900 DIALYZER |
Applicant |
ERIKA, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
ERIKA, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 876.5820
|
Classification Product Code |
|
Date Received | 09/22/1976 |
Decision Date | 11/19/1976 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|