The following data is part of a premarket notification filed by Kulzer, Inc. with the FDA for Estilux(r) Posterior C.
| Device ID | K863314 |
| 510k Number | K863314 |
| Device Name: | ESTILUX(R) POSTERIOR C |
| Classification | Material, Tooth Shade, Resin |
| Applicant | KULZER, INC. 111 N. WABASH AVE. Chicago, IL 60602 |
| Contact | Bauer, Phd |
| Correspondent | Bauer, Phd KULZER, INC. 111 N. WABASH AVE. Chicago, IL 60602 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-08-26 |
| Decision Date | 1986-09-22 |