The following data is part of a premarket notification filed by Ivoclar Vivadent, Inc. with the FDA for Sr Phonares Nhc.
| Device ID | K093331 |
| 510k Number | K093331 |
| Device Name: | SR PHONARES NHC |
| Classification | Denture, Plastic, Teeth |
| Applicant | IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Donna Marie Hartnett |
| Correspondent | Donna Marie Hartnett IVOCLAR VIVADENT, 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 | 2009-10-26 |
| Decision Date | 2010-01-28 |