The following data is part of a premarket notification filed by J.f. Jelenko & Co., Inc. with the FDA for Diamond (code Name Pt-054).
| Device ID | K960403 |
| 510k Number | K960403 |
| Device Name: | DIAMOND (CODE NAME PT-054) |
| Classification | Alloy, Gold-based Noble Metal |
| Applicant | J.F. JELENKO & CO., INC. 99 BUSINESS PARK DR. Armonk, NY 10504 |
| Contact | Tridib Dasgupta |
| Correspondent | Tridib Dasgupta J.F. JELENKO & CO., INC. 99 BUSINESS PARK DR. Armonk, NY 10504 |
| Product Code | EJT |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-29 |
| Decision Date | 1996-02-26 |