The following data is part of a premarket notification filed by J.f. Jelenko & Co., Inc. with the FDA for Jel 15.
| Device ID | K000532 |
| 510k Number | K000532 |
| Device Name: | JEL 15 |
| Classification | Alloy, Other Noble Metal |
| Applicant | J.F. JELENKO & CO., INC. 99 BUSINESS PARK DR. Armonk, NY 10504 |
| Contact | Raphael Judkins |
| Correspondent | Raphael Judkins 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 | 2000-02-17 |
| Decision Date | 2000-04-06 |