Device Classification Name |
oximeter
|
510(k) Number |
K863918 |
Device Name |
MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT. |
Applicant |
MARQUEST MEDICAL PRODUCTS, INC. |
11039 EAST LANSING CIR. |
ENGLEWOOD,
CO
80112
|
|
Applicant Contact |
R. J MCKINNON |
Correspondent |
MARQUEST MEDICAL PRODUCTS, INC. |
11039 EAST LANSING CIR. |
ENGLEWOOD,
CO
80112
|
|
Correspondent Contact |
R. J MCKINNON |
Regulation Number | 870.2700
|
Classification Product Code |
|
Date Received | 10/08/1986 |
Decision Date | 01/07/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|