The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Dw231 Dental Alloy.
| Device ID | K902376 |
| 510k Number | K902376 |
| Device Name: | DW231 DENTAL ALLOY |
| Classification | Alloy, Other Noble Metal |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | L Severance,dds |
| Correspondent | L Severance,dds IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | EJS |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-05-29 |
| Decision Date | 1990-06-28 |