The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Dw 236.
| Device ID | K905204 |
| 510k Number | K905204 |
| Device Name: | DW 236 |
| Classification | Alloy, Amalgam |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Gary L Severance |
| Correspondent | Gary L Severance IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | EJJ |
| CFR Regulation Number | 872.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-11-20 |
| Decision Date | 1991-03-29 |