Yeti Dentalprodukte GmbH · Class II · Cleared Nov 15, 2018
| K-number | K173971 |
| Device name | K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent |
| Applicant | Yeti Dentalprodukte GmbH |
| Product code | EIH |
| Device class | Class II |
| Decision date | Nov 15, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 872.6660 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov