Device Classification Name |
material, impression
|
510(k) Number |
K963609 |
Device Name |
PHASE PLUS |
Applicant |
ZHERMACK S.P.A. |
7527 WESTMORELAND AVE. |
ST. LOUIS,
MO
63105
|
|
Applicant Contact |
EVAN DICK |
Correspondent |
ZHERMACK S.P.A. |
7527 WESTMORELAND AVE. |
ST. LOUIS,
MO
63105
|
|
Correspondent Contact |
EVAN DICK |
Regulation Number | 872.3660
|
Classification Product Code |
|
Date Received | 09/10/1996 |
Decision Date | 11/14/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Dental
|
510k Review Panel |
Dental
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|