# K973701: Somnus Tissue Coagulating Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Somnus Medical Technologies, Inc.
- Decided: Jan 30, 1998 after 123 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
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) Somnus Medical Technologies, Inc. Tissue Coagulating Electrodes: named in the summary without a submission number

## Indications for use
The Somnus Model RC-1 and RC-2 Reusable Cables are intended to provide an electrical connection between the Somnne Medical Technologies Madel 1100, 1110 and 2119 Tissue Coagulating Electrodes and the Somnus Medical Technologies Electrosurgical (RF) Generators

Source page: https://510kreport.com/device/K973701
Methodology: https://510kreport.com/methodology