# K111355: Echobright

- Pathway: 510(k) (Special)
- Applicant: Life-Tech, Inc.
- Decided: Sep 16, 2011 after 123 days
- Product code: CAZ (Anesthesia Conduction Kit)
- Device class: 2
- Regulation: 21 CFR 868.5140
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K143164: ON-Q Pain Relief System, QuikBloc Over-the-Needle Catheter Set (2014), 4 descendants of its own
- K152952: E-Cath (2016), 1 descendant of its own
- K202699: E-Cath STIM acc. Tsui (2020), 0 descendants of its own
- K171193: Certa Catheter (2017), 0 descendants of its own
- K161232: ON-Q* EchoSpark Echogenic Catheter; ON-Q* T-bloc* Echogenic Continuous Nerve Block Kit (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K111355
Methodology: https://510kreport.com/methodology