# K951032: Finess I (Dermatologic Application)

- Pathway: 510(k) (Traditional)
- Applicant: Utah Medical Products, Inc.
- Decided: Apr 6, 1995 after 31 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K123310: Finesse 3RD Generation (Models Finesse+ and Finesseii+) (2013), 1 descendant of its own
- K133273: Liger Medical Esu-110 (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K951032
Methodology: https://510kreport.com/methodology