# K042900: K.E.P. Connector and Clip

- Pathway: 510(k) (Traditional)
- Applicant: K.E.P., LLC
- Decided: Nov 5, 2004 after 17 days
- Product code: KDJ (Set, Administration, For Peritoneal Dialysis, Disposable)
- Device class: 2
- Regulation: 21 CFR 876.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The K.E.P. Connector and Clip is intended to secure the position of the outlet tubing of single-use peritoneal dialysis sets on any solid surface.

Source page: https://510kreport.com/device/K042900
Methodology: https://510kreport.com/methodology