The following data is part of a premarket notification filed by Jeneric/pentron, Inc. with the FDA for Avante Curelight.
| Device ID | K003683 |
| 510k Number | K003683 |
| Device Name: | AVANTE CURELIGHT |
| Classification | Activator, Ultraviolet, For Polymerization |
| Applicant | JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 -0724 |
| Contact | Annmarie Tenero |
| Correspondent | Annmarie Tenero JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL RD. P.O. BOX 724 Wallingford, CT 06492 -0724 |
| Product Code | EBZ |
| CFR Regulation Number | 872.6070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-11-29 |
| Decision Date | 2001-01-11 |