The following data is part of a premarket notification filed by Kuraray Co. with the FDA for Clearfil Posterior 3.
| Device ID | K871635 |
| 510k Number | K871635 |
| Device Name: | CLEARFIL POSTERIOR 3 |
| Classification | Material, Tooth Shade, Resin |
| Applicant | KURARAY CO. 875 AVENUE OF THE AMERICAS New York, NY 10001 |
| Contact | Paul Roberts |
| Correspondent | Paul Roberts KURARAY CO. 875 AVENUE OF THE AMERICAS New York, NY 10001 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-27 |
| Decision Date | 1987-07-16 |