The following data is part of a premarket notification filed by Aurex Precious Metal Industries (pty)ltd with the FDA for Aurecast 4.
Device ID | K972937 |
510k Number | K972937 |
Device Name: | AURECAST 4 |
Classification | Alloy, Gold-based Noble Metal |
Applicant | AUREX PRECIOUS METAL INDUSTRIES (PTY)LTD P.O. BOX 509 Edenvale, ZA 1610 |
Contact | J.d. Davis |
Correspondent | J.d. Davis AUREX PRECIOUS METAL INDUSTRIES (PTY)LTD P.O. BOX 509 Edenvale, ZA 1610 |
Product Code | EJT |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-20 |
Decision Date | 1997-08-25 |
Summary: | summary |