# K061183: Confluent Surgical Dual Liquid Applicator, Model 70-2005-093

- Pathway: 510(k) (Special)
- Applicant: Confluent Surgical,Inc
- Decided: Jun 1, 2006 after 34 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
Longest line of descent: 1 generation back to K042588 (2004). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
1 of 4 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042588: Confluent Surgical Dual Liquid Applicator, Model 70-2005093, Confluent Surgical,Inc (2004) Summary page 1.

## Most influential descendants
- K072790: Confluent Surgical Extended Tip Applicator, Model 70-2008-008 (2008), 1 descendant of its own
- K091315: Covidien Extended Tip Applicator (2009), 0 descendants of its own

## Indications for use
The Confluent Surgical Dual Liquid Applicator is indicated for use in the simultaneous delivery of two non-homogenous fluids or solutions onto a surgical site.

Source page: https://510kreport.com/device/K061183
Methodology: https://510kreport.com/methodology