The following data is part of a premarket notification filed by Jeneric/pentron, Inc. with the FDA for Avante Micro Crystal System.
| Device ID | K012231 |
| 510k Number | K012231 |
| Device Name: | AVANTE MICRO CRYSTAL SYSTEM |
| Classification | Powder, Porcelain |
| Applicant | JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL ROAD Wallingford, CT 06492 -0724 |
| Contact | Annmarie Tenero |
| Correspondent | Annmarie Tenero JENERIC/PENTRON, INC. 53 NORTH PLAINS INDUSTRIAL ROAD Wallingford, CT 06492 -0724 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-07-16 |
| Decision Date | 2001-08-23 |
| Summary: | summary |