The following data is part of a premarket notification filed by J. Aderer, Inc. with the FDA for Duallor 'r'.
| Device ID | K821572 |
| 510k Number | K821572 |
| Device Name: | DUALLOR 'R' |
| Classification | Alloy, Other Noble Metal |
| Applicant | J. ADERER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EJS |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-27 |
| Decision Date | 1982-06-14 |