The following data is part of a premarket notification filed by Vident with the FDA for Vita Cerec Set And Vita Cerec Blocs.
| Device ID | K895901 |
| 510k Number | K895901 |
| Device Name: | VITA CEREC SET AND VITA CEREC BLOCS |
| Classification | Material, Impression |
| Applicant | VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Contact | Ray E Morrow |
| Correspondent | Ray E Morrow VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-06 |
| Decision Date | 1992-01-17 |