| Device Classification Name |
Alloy, Amalgam
|
| 510(k) Number |
K933309 |
| Device Name |
PRINCE |
| Applicant |
| Goldsmith & Revere, Inc. |
| 242 S. Dean St. |
|
Englewood,
NJ
07631
|
|
| Applicant Contact |
TIM WOLF |
| Correspondent |
| Goldsmith & Revere, Inc. |
| 242 S. Dean St. |
|
Englewood,
NJ
07631
|
|
| Correspondent Contact |
TIM WOLF |
| Regulation Number | 872.3070 |
| Classification Product Code |
|
| Date Received | 07/07/1993 |
| Decision Date | 10/01/1993 |
| Decision |
Substantially Equivalent
(SESE) |
| Regulation Medical Specialty |
Dental
|
| 510k Review Panel |
Dental
|
| Type |
Traditional
|
| Reviewed by Third Party |
No
|
| Combination Product |
No
|
Predetermined Change Control Plan Authorized |
No
|
|
|