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 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10841396117739 | K820181 | 000 |
| 10841396117630 | K820181 | 000 |
| 10841396117647 | K820181 | 000 |
| 10841396117654 | K820181 | 000 |
| 10841396117661 | K820181 | 000 |
| 10841396117678 | K820181 | 000 |
| 10841396117685 | K820181 | 000 |
| 10841396117692 | K820181 | 000 |
| 10841396117708 | K820181 | 000 |
| 10841396117715 | K820181 | 000 |
| 10841396117722 | K820181 | 000 |
| 10841396117623 | K820181 | 000 |