Device Classification Name |
Spirometer, Diagnostic
|
510(k) Number |
K920111 |
Device Name |
SENSORMEDICS MODEL 2130 SPIEOMETRY SYSTEM |
Applicant |
SENSORMEDICS CORP. |
22705 SAVI RANCH PKWY. |
YORBA LINDA,
CA
92887 -4645
|
|
Applicant Contact |
PAUL L KITTINGER |
Correspondent |
SENSORMEDICS CORP. |
22705 SAVI RANCH PKWY. |
YORBA LINDA,
CA
92887 -4645
|
|
Correspondent Contact |
PAUL L KITTINGER |
Regulation Number | 868.1840
|
Classification Product Code |
|
Date Received | 01/10/1992 |
Decision Date | 10/26/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|