K190091 is an FDA 510(k) clearance for the Diapaste. This device is classified as a Resin, Root Canal Filling (Class II - Special Controls, product code KIF).
Submitted by DiaDent Group International (Cheongju-Si, KR). The FDA issued a Cleared decision on March 27, 2020, 434 days after receiving the submission on January 18, 2019.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3820.
| 510(k) Number | K190091 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 18, 2019 |
| Decision Date | March 27, 2020 |
| Days to Decision | 434 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | KIF — Resin, Root Canal Filling |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3820 |