Device Classification Name |
display, cathode-ray tube, medical
|
510(k) Number |
K760523 |
Device Name |
MONITOR SCOPE |
Applicant |
HEWLETT-PACKARD CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
HEWLETT-PACKARD CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 870.2450
|
Classification Product Code |
|
Date Received | 08/26/1976 |
Decision Date | 09/03/1976 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|