# K000456: Harvest Technologies Dual Liquid Applicator, Model SK/S:  Harvest Dual Liquid Applicator LK/2

- Pathway: 510(k) (Traditional)
- Applicant: Harvest Technologies, LLC
- Decided: Jun 1, 2000 after 111 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- 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
- K020147: Magellan Ratio Dispenser Kit/Magellan Spray Tip/Magellan Cannula Tip (2002), 1 descendant of its own
- K041830: Magellan Ratio Dispenser Kit (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K000456
Methodology: https://510kreport.com/methodology