# K955035: Vidamed Series 7205 Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Vidamed, Inc.
- Decided: Nov 29, 1995 after 27 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.
21 later devices descend from it; 2 cite it directly.
0 of 22 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
- K960918: Vidamed Tuna (Transurethral Needle Ablation) System (1996), 19 descendants of its own
- K963180: Vidamed RF Generator Data Recorder (1996), 13 descendants of its own
- K965061: Vidamed Modedl 7600 RF Generator (1997), 12 descendants of its own
- K052413: Tuna System, Models 8909, 8929, 8930, 8934 (2005), 10 descendants of its own
- K113380: Prostiva RF Therapy Hand Piece Prostiva RF Therapy RF Generator (2012), 9 descendants of its own

Source page: https://510kreport.com/device/K955035
Methodology: https://510kreport.com/methodology