# K983081: Begopal 300

- Pathway: 510(k) (Traditional)
- Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
- Decided: Oct 28, 1998 after 56 days
- Product code: EJS (Alloy, Other 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
BegoPal 300 is a crown and bridge metal to ceramic type 4 alloy. It is a medical device in accordance with Regulation 93/42 EEG. Class 1la according to Annex IX. The CE seal of approval is confirmation of the fact that the regulaiton requirements are met.

Source page: https://510kreport.com/device/K983081
Methodology: https://510kreport.com/methodology