# K951927: Combined End-Multiple Lateral Holes Epidural Catheter (Cemlh Epidural Catheter)

- Pathway: 510(k) (Traditional)
- Applicant: Csen, Ltd.
- Decided: May 30, 1997 after 767 days
- Product code: BSO (Catheter, Conduction, Anesthetic)
- Device class: 2
- Regulation: 21 CFR 868.5120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K042488: Perifix Catheter and Contiplex Catheter (2004), 9 descendants of its own
- K043500: Functional Anaesthetic Discography (Fad) System, Including Fad Catheter Kit and Fad Introducer Needle (2005), 3 descendants of its own
- K061210: Functional  Anaesthetic Discography (Fad) Catheter System, Model D01A ; Introducer Needle, Model D01B (2006), 2 descendants of its own
- K063071: Discyphor Catheter System, Model D01A; Discyphor Introducer Needle, Model D01B (2007), 1 descendant of its own
- K153297: Perifix and Contiplex Catheter (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K951927
Methodology: https://510kreport.com/methodology