# K143536: Voyant Fine Fusion Device

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Resources
- Decided: Apr 16, 2015 after 122 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: 4 generations back to K932293 (1994). 11 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102470: Lugasure Curved, Small Jaw, Open Sealer/Divider, Covidien, Formerly Valleylab, (2011) Summary page 4.

## Most influential descendants
- K153017: Voyant Fine Fusion (2016), 1 descendant of its own
- K202818: Voyant Fine Fusion Device (EB230) (2021), 0 descendants of its own

## Indications for use
The Voyant Fine Fusion is a bipolar, electrosurgical device indicated for use with the Voyant electrosurgical generator in open procedures where the ligation and division of vessels and tissue bundles is desired. The device can seal and divide vessels up to and including 3mm in diameter and tissue bundles that can be captured in the jaws of the device. The device has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures, and should not be used for these procedures.

Source page: https://510kreport.com/device/K143536
Methodology: https://510kreport.com/methodology