The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Sybron/kerr Contour.
| Device ID | K820181 |
| 510k Number | K820181 |
| Device Name: | SYBRON/KERR CONTOUR |
| Classification | Alloy, Amalgam |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EJJ |
| CFR Regulation Number | 872.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-22 |
| Decision Date | 1982-02-24 |