Device Classification Name |
nebulizer (direct patient interface)
|
510(k) Number |
K010680 |
Device Name |
CT SPACER |
Applicant |
CLINICAL TECHNOLOGIES, INC. |
705 E. VIRGINIA WAY |
SUITE 1 |
BARSTOW,
CA
92311
|
|
Applicant Contact |
BOB JOHNSON |
Correspondent |
CLINICAL TECHNOLOGIES, INC. |
705 E. VIRGINIA WAY |
SUITE 1 |
BARSTOW,
CA
92311
|
|
Correspondent Contact |
BOB JOHNSON |
Regulation Number | 868.5630
|
Classification Product Code |
|
Date Received | 03/07/2001 |
Decision Date | 05/23/2001 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|