Device Classification Name |
Syringe, Piston
|
510(k) Number |
K894335 |
Device Name |
MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR |
Applicant |
MIDMARK CORP. |
60 VISTA DR. |
P.O. BOX 286 |
VERSAILLES,
OH
45380
|
|
Applicant Contact |
JOHN OLDIGES |
Correspondent |
MIDMARK CORP. |
60 VISTA DR. |
P.O. BOX 286 |
VERSAILLES,
OH
45380
|
|
Correspondent Contact |
JOHN OLDIGES |
Regulation Number | 880.5860
|
Classification Product Code |
|
Date Received | 07/14/1989 |
Decision Date | 09/12/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|