Device Classification Name |
System, Dialysate Delivery, Central Multiple Patient
|
510(k) Number |
K842225 |
Device Name |
HEMODIAL CONCENTRATE MIXING APPARATUS |
Applicant |
LMF MEDICAL RESEARCH & MANUFACTURING, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
LMF MEDICAL RESEARCH & MANUFACTURING, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 876.5820
|
Classification Product Code |
|
Date Received | 06/05/1984 |
Decision Date | 10/02/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|