Device Classification Name |
Nebulizer (Direct Patient Interface)
|
510(k) Number |
K923690 |
Device Name |
MINI HEART |
Applicant |
B & B MEDICAL TECHNOLOGIES, INC. |
3569 RECYCLE RD., SUITE 16 |
RANCHO CORDOVA,
CA
95670
|
|
Applicant Contact |
BRIGGS II |
Correspondent |
B & B MEDICAL TECHNOLOGIES, INC. |
3569 RECYCLE RD., SUITE 16 |
RANCHO CORDOVA,
CA
95670
|
|
Correspondent Contact |
BRIGGS II |
Regulation Number | 868.5630
|
Classification Product Code |
|
Date Received | 07/24/1992 |
Decision Date | 10/20/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|