The following data is part of a premarket notification filed by J.f. Jelenko & Co., Inc. with the FDA for Silcast (code Name Rd-0118).
Device ID | K981247 |
510k Number | K981247 |
Device Name: | SILCAST (CODE NAME RD-0118) |
Classification | Alloy, Other 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 | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-04-06 |
Decision Date | 1998-07-01 |