# K042588: Confluent Surgical Dual Liquid Applicator, Model 70-2005093

- Pathway: 510(k) (Traditional)
- Applicant: Confluent Surgical,Inc
- Decided: Dec 9, 2004 after 78 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.
3 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)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K872526: CT Pace Catalog Number B7950A, General Electric Co. (1987). Our reading of the summary gave K872526, FDA’s number for CT Pace Catalog Number B7950A (General Electric Co.). Its FDA name has none of the distinctive words the summary uses for the device it names, “DuoFlo Dispenser Kit”. Kept off the family tree. Summary page 1.

## Most influential descendants
- K061183: Confluent Surgical Dual Liquid Applicator, Model 70-2005-093 (2006), 2 descendants of its own
- 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-homogeneous fluids or solutions onto a surgical site.

Source page: https://510kreport.com/device/K042588
Methodology: https://510kreport.com/methodology