# K972951: Hipallaur 51

- Pathway: 510(k) (Traditional)
- Applicant: Aurex Precious Metal Industries (Pty)Ltd
- Decided: Sep 5, 1997 after 77 days
- Product code: EJT (Alloy, Gold-Based Noble Metal)
- Device class: 2
- Regulation: 21 CFR 872.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Jelenko Cameo: named in the summary without a submission number

## Indications for use
Dental casting alloy used in combination with dental ceramics for fabrication of metallo-ceramic restoration.

Source page: https://510kreport.com/device/K972951
Methodology: https://510kreport.com/methodology