The following data is part of a premarket notification filed by Pentron Clinical with the FDA for Correct Plus 1.
| Device ID | K130920 |
| 510k Number | K130920 |
| Device Name: | CORRECT PLUS 1 |
| Classification | Material, Impression |
| Applicant | PENTRON CLINICAL 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Contact | Wendy Garman |
| Correspondent | Wendy Garman PENTRON CLINICAL 1717 WEST COLLINS AVENUE Orange, CA 92867 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-04-03 |
| Decision Date | 2013-07-02 |
| Summary: | summary |