The following data is part of a premarket notification filed by J.f. Jelenko & Co., Inc. with the FDA for Benchmark Iii.
| Device ID | K922447 |
| 510k Number | K922447 |
| Device Name: | BENCHMARK III |
| Classification | Alloy, Other Noble Metal |
| Applicant | J.F. JELENKO & CO., INC. 99 BUSINESS PARK DR. Armonk, NY 10504 |
| Contact | Costantino Volpe |
| Correspondent | Costantino Volpe J.F. JELENKO & CO., INC. 99 BUSINESS PARK DR. Armonk, NY 10504 |
| Product Code | EJS |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-05-22 |
| Decision Date | 1992-08-05 |