| Device Classification Name |
cement, dental |
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|---|---|---|---|---|
| 510(k) Number | K991974 | |||
| Device Name | FUTURA GLASS IONOMER SILVER REINFORCED | |||
| Applicant |
|
|||
| Applicant Contact | clyde e ingersoll | |||
| Correspondent |
|
|||
| Correspodent Contact | clyde e ingersoll | |||
| Regulation Number | 872.3275 | |||
| Classification Product Code |
|
|||
| Date Received | 06/11/1999 | |||
| Decision Date | 09/17/1999 | |||
| Decision |
substantially equivalent (SESE) |
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| Regulation Medical Specialty |
Dental |
|||
| 510k Review Panel |
Dental |
|||
| statement |
statement |
|||
| Type | Traditional | |||
| Reviewed by Third Party | No | |||
| Combination Product |
No |