Device Classification Name |
container, i.v.
|
510(k) Number |
K811269 |
Device Name |
GLASS VIALS |
Applicant |
MEDI-PLAST INTL., INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
MEDI-PLAST INTL., INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 880.5025
|
Classification Product Code |
|
Date Received | 05/05/1981 |
Decision Date | 06/16/1981 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|