Device Classification Name |
Nebulizer (Direct Patient Interface)
|
510(k) Number |
K874047 |
Device Name |
ASTHMAKIT |
Applicant |
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. |
DIVISION OF DIEMOLDING CORP. |
CANASTOTA,
NY
13032
|
|
Applicant Contact |
RONALD N MCHENRY |
Correspondent |
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. |
DIVISION OF DIEMOLDING CORP. |
CANASTOTA,
NY
13032
|
|
Correspondent Contact |
RONALD N MCHENRY |
Regulation Number | 868.5630
|
Classification Product Code |
|
Date Received | 10/05/1987 |
Decision Date | 02/29/1988 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|