# K823924: Model SSE4 Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Valleylab, Inc.
- Decided: Jan 9, 1983 after 12 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.
20 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K980366: Aaron 1200 High Frequency Electrosurgicl Generator A1200, A1200/240 (1998), 19 descendants of its own
- K021817: Aaron A950 High Frequency Electrosurgical Generator, Aaron A950 Electrosurgical Generator, 240V (2002), 16 descendants of its own
- K161134: Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator (2016), 14 descendants of its own
- K192813: Plasma IQ (2020), 12 descendants of its own
- K212329: Plasma IQ (2021), 5 descendants of its own

Source page: https://510kreport.com/device/K823924
Methodology: https://510kreport.com/methodology