Device Classification Name |
Oximeter
|
510(k) Number |
K943817 |
Device Name |
MARQUETTE ADULT/NEONATAL WRAP SENSOR |
Applicant |
MARQUETTE ELECTRONICS, INC. |
100 MARQUETTE DR. |
JUPITER,
FL
33468
|
|
Applicant Contact |
DAVID A LOVEJOY |
Correspondent |
MARQUETTE ELECTRONICS, INC. |
100 MARQUETTE DR. |
JUPITER,
FL
33468
|
|
Correspondent Contact |
DAVID A LOVEJOY |
Regulation Number | 870.2700
|
Classification Product Code |
|
Date Received | 08/05/1994 |
Decision Date | 10/18/1994 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|