# K994173: Stellartech Radiofrequency Generator,Model 1025A-115, Stellartech Radiofrequency Generator, Model 1025A-230

- Pathway: 510(k) (Abbreviated)
- Applicant: Stellartech Research Corp.
- Decided: Jan 20, 2000 after 41 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: 1 generation back to K981672 (1998). 1 ancestor in all.
44 later devices descend from it; 3 cite it directly.
0 of 46 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981672: Radiotherapeutics RF-2000 Radiofrequency Generator, Radiotherapeutics Corp. (1998) Summary page 1.

## Most influential descendants
- K023765: Stellartech Coagulation System (Models 1100C-115 & 1100C-230) (2002), 42 descendants of its own
- K013139: Stellartech Coagulation System (2001), 42 descendants of its own
- K032062: Stellartech Coagulation System, Models  (1100C-115 & 1100C-230) (2003), 41 descendants of its own
- K032452: Modification to: Stellartech Coagulation System, Models 1100C-115 & 100C-230 (2003), 39 descendants of its own
- K032721: Modification to: Stellartech Coagulation System (Models 1100C-115 & 1100C-230) (2003), 38 descendants of its own

## Indications for use
The Stellartech Radio Frequency Generator (Model 1025A-115 and Model 1025A-230) is indicated for use in general surgical procedures to cut and coagulate soft tissue.

Source page: https://510kreport.com/device/K994173
Methodology: https://510kreport.com/methodology