The following data is part of a premarket notification filed by Kavo America Corporation with the FDA for Kavo Everest Zh-blank.
| Device ID | K033221 |
| 510k Number | K033221 |
| Device Name: | KAVO EVEREST ZH-BLANK |
| Classification | Powder, Porcelain |
| Applicant | KAVO AMERICA CORPORATION PO BOX 7007 Deerfield, IL 60015 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm KAVO AMERICA CORPORATION PO BOX 7007 Deerfield, IL 60015 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-10-03 |
| Decision Date | 2003-10-28 |
| Summary: | summary |