The following data is part of a premarket notification filed by Jeneric/pentron, Inc. with the FDA for Quell Desensitizer.
| Device ID | K010957 |
| 510k Number | K010957 |
| Device Name: | QUELL DESENSITIZER |
| Classification | Varnish, Cavity |
| 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 | LBH |
| CFR Regulation Number | 872.3260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-03-30 |
| Decision Date | 2001-06-25 |