Device Classification Name |
connector, airway (extension)
|
510(k) Number |
K922537 |
Device Name |
DURALIFE |
Applicant |
DHD DIEMOLDING HEALTHCARE DIV. |
125 RASBACH ST. |
CANASTOTA,
NY
13032
|
|
Applicant Contact |
JEAN WALLACE |
Correspondent |
DHD DIEMOLDING HEALTHCARE DIV. |
125 RASBACH ST. |
CANASTOTA,
NY
13032
|
|
Correspondent Contact |
JEAN WALLACE |
Regulation Number | 868.5810
|
Classification Product Code |
|
Date Received | 05/28/1992 |
Decision Date | 12/04/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|