K200614 is an FDA 510(k) clearance for the FiteBac Antimicrobial Cavity Cleanser. This device is classified as a Varnish, Cavity (Class II - Special Controls, product code LBH).
Submitted by Largent Health, LLC (Marietta, US). The FDA issued a Cleared decision on June 25, 2020, 108 days after receiving the submission on March 9, 2020.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3260.
| 510(k) Number | K200614 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 09, 2020 |
| Decision Date | June 25, 2020 |
| Days to Decision | 108 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | LBH - Varnish, Cavity |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3260 |