K212939 is an FDA 510(k) clearance for the Vintage Prime Press. This device is classified as a Powder, Porcelain (Class II - Special Controls, product code EIH).
Submitted by Shofu Dental Corporation (San Marcos, US). The FDA issued a Cleared decision on March 18, 2022, 184 days after receiving the submission on September 15, 2021.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6660.
| 510(k) Number | K212939 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 15, 2021 |
| Decision Date | March 18, 2022 |
| Days to Decision | 184 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EIH — Powder, Porcelain |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6660 |