The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Dw 273 #1.
| Device ID | K003632 |
| 510k Number | K003632 |
| Device Name: | DW 273 #1 |
| Classification | Alloy, Other Noble Metal |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Andy Gulati |
| Correspondent | Andy Gulati 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 | 2000-11-24 |
| Decision Date | 2000-12-20 |