# K032062: Stellartech Coagulation System, Models  (1100C-115 & 1100C-230)

- Pathway: 510(k) (Special)
- Applicant: Stellartech Research Corp.
- Decided: Jul 29, 2003 after 26 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: 6 generations back to K943450 (1995). 23 ancestors in all.
41 later devices descend from it; 7 cite it directly.
0 of 65 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K834413: Dilation Balloon Catheter, Hobbs Medical, Inc. (1984) Summary page 1.
- K013139: Stellartech Coagulation System, Stellartech Research Corp. (2001)
- K023765: Stellartech Coagulation System (Models 1100C-115 & 1100C-230), Stellartech Research Corp. (2002) Summary page 1.

## Most influential descendants
- 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
- K040240: Stellartech Coagulation System (Models 1100C-115 & 1100C-230) (2004), 37 descendants of its own
- K041383: Stellartech Coagulation System, Models 1100C-115 and 1100C-230 (2004), 36 descendants of its own
- K042909: Stellartech Coagulation System, Models 1100C-115A & 1100C-230A (2004), 35 descendants of its own

## Indications for use
The Stellartech Coagulation System is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including but not limited to, the esophagus. Indications include Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett’s Esophagus, Dieulafoy Lesions, and Angiodysplasia.

Source page: https://510kreport.com/device/K032062
Methodology: https://510kreport.com/methodology