The following data is part of a premarket notification filed by Hoyt Laboratories with the FDA for Replica Dental Composit.
| Device ID | K771880 |
| 510k Number | K771880 |
| Device Name: | REPLICA DENTAL COMPOSIT |
| Classification | Material, Tooth Shade, Resin |
| Applicant | HOYT LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-10-04 |
| Decision Date | 1977-10-20 |