Device Classification Name |
Oximeter
|
510(k) Number |
K020350 |
Device Name |
BCI 3180 PULSE OXIMETER |
Applicant |
BCI, INC. |
N7 W22025 JOHNSON RD. |
WAUKESHA,
WI
53186
|
|
Applicant Contact |
DONALD ALEXANDER |
Correspondent |
BCI, INC. |
N7 W22025 JOHNSON RD. |
WAUKESHA,
WI
53186
|
|
Correspondent Contact |
DONALD ALEXANDER |
Regulation Number | 870.2700
|
Classification Product Code |
|
Date Received | 02/04/2002 |
Decision Date | 04/30/2002 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|