Device Classification Name |
pump, infusion
|
510(k) Number |
K061128 |
Device Name |
MODIFICATION TO MEDRAD CONTINUUM MR INFUSION SYSTEM |
Applicant |
MEDRAD, INC. |
ONE MEDRAD DR. |
INDIANOLA,
PA
15051
|
|
Applicant Contact |
JOHN M KISTE |
Correspondent |
MEDRAD, INC. |
ONE MEDRAD DR. |
INDIANOLA,
PA
15051
|
|
Correspondent Contact |
JOHN M KISTE |
Regulation Number | 880.5725
|
Classification Product Code |
|
Date Received | 04/24/2006 |
Decision Date | 05/22/2006 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|