K003683 is an FDA 510(k) clearance for the AVANTE CURELIGHT. This device is classified as a Activator, Ultraviolet, For Polymerization (Class II - Special Controls, product code EBZ).
Submitted by Jeneric/Pentron, Inc. (Wallingford, US). The FDA issued a Cleared decision on January 11, 2001, 43 days after receiving the submission on November 29, 2000.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6070.
| 510(k) Number | K003683 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 29, 2000 |
| Decision Date | January 11, 2001 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBZ — Activator, Ultraviolet, For Polymerization |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6070 |