Device Classification Name |
Oximeter
|
510(k) Number |
K071610 |
Device Name |
MEDIAID PULSE OXIMETER M30 AND M34 |
Applicant |
MEDIAID INC. |
17517 FABRICA WAY, SUITE H |
CERRITOS,
CA
90703
|
|
Applicant Contact |
JAYESH PATEL |
Correspondent |
MEDIAID INC. |
17517 FABRICA WAY, SUITE H |
CERRITOS,
CA
90703
|
|
Correspondent Contact |
JAYESH PATEL |
Regulation Number | 870.2700
|
Classification Product Code |
|
Date Received | 06/13/2007 |
Decision Date | 11/05/2007 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|