The following data is part of a premarket notification filed by Jeneric Ind. with the FDA for Luxor Porcelain.
| Device ID | K820057 |
| 510k Number | K820057 |
| Device Name: | LUXOR PORCELAIN |
| Classification | Powder, Porcelain |
| Applicant | JENERIC IND. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-11 |
| Decision Date | 1982-03-02 |