K083036 is an FDA 510(k) clearance for the VOCO PROFLUORID L. This device is classified as a Varnish, Cavity (Class II - Special Controls, product code LBH).
Submitted by Voco GmbH (Cuxhaven, DE). The FDA issued a Cleared decision on January 12, 2009, 90 days after receiving the submission on October 14, 2008.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3260.
| 510(k) Number | K083036 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 14, 2008 |
| Decision Date | January 12, 2009 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | LBH — Varnish, Cavity |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3260 |