The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Sr Antaris Anterior Teeth/sr Postaris Posterior Teeth.
| Device ID | K962456 |
| 510k Number | K962456 |
| Device Name: | SR ANTARIS ANTERIOR TEETH/SR POSTARIS POSTERIOR TEETH |
| Classification | Denture, Plastic, Teeth |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Peter P Mancuso |
| Correspondent | Peter P Mancuso IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | ELM |
| CFR Regulation Number | 872.3590 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-25 |
| Decision Date | 1996-08-06 |