The following data is part of a premarket notification filed by Adp Intl., Inc. with the FDA for Dental Alloy.
| Device ID | K760980 |
| 510k Number | K760980 |
| Device Name: | DENTAL ALLOY |
| Classification | Alloy, Amalgam |
| Applicant | ADP INTL., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EJJ |
| CFR Regulation Number | 872.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-10-21 |
| Decision Date | 1976-11-15 |