The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Coreform Molds.
| Device ID | K801530 |
| 510k Number | K801530 |
| Device Name: | COREFORM MOLDS |
| Classification | Instruments, Dental Hand |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DZN |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-02 |
| Decision Date | 1980-07-28 |