# K233002: Beed 2,5, Beed 3,8

- Pathway: 510(k) (Traditional)
- Applicant: Excelsior Resources, LLC
- Decided: Mar 20, 2024 after 180 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K780977 (1978). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960255: Ceramic Blade Electrode, Utah Medical Products, Inc. (1996) Summary page 4.

## Indications for use
The BEED 3,8 and BEED 2,5 device are used for electrosurgical cutting and coagulation through tissues, or within tissue planes while maintaining hemostasis.

Source page: https://510kreport.com/device/K233002
Methodology: https://510kreport.com/methodology