# K072790: Confluent Surgical Extended Tip Applicator, Model 70-2008-008

- Pathway: 510(k) (Traditional)
- Applicant: Confluent Surgical,Inc
- Decided: Jan 11, 2008 after 102 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: 2 generations back to K042588 (2004). 2 ancestors in all.
1 later device descends 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)
- K061183: Confluent Surgical Dual Liquid Applicator, Model 70-2005-093, Confluent Surgical,Inc (2006) Summary page 1.

## Most influential descendants
- K091315: Covidien Extended Tip Applicator (2009), 0 descendants of its own

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

Source page: https://510kreport.com/device/K072790
Methodology: https://510kreport.com/methodology