The following data is part of a premarket notification filed by Nobelpharma Usa, Inc. with the FDA for Procera All-ceramic Porcelain.
| Device ID | K944702 |
| 510k Number | K944702 |
| Device Name: | PROCERA ALL-CERAMIC PORCELAIN |
| Classification | Powder, Porcelain |
| Applicant | NOBELPHARMA USA, INC. 777 OAKMONT LN. SUITE 100 Westmont, IL 60559 |
| Contact | Mary Edwards |
| Correspondent | Mary Edwards NOBELPHARMA USA, INC. 777 OAKMONT LN. SUITE 100 Westmont, IL 60559 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-09-22 |
| Decision Date | 1994-12-02 |