# K091670: BD L-Cath Single and Dual Lument Catheters, Midline Catheter

- Pathway: 510(k) (Special)
- Applicant: Becton, Dickinson & CO
- Decided: Jul 1, 2009 after 22 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K925979 (1993). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925979: Dual Lumen L-Cath Catheter System, Luther Medical Products, Inc. (1993) Summary page 1.
- K920755: L-Cath Peel Away System Catheter, Luther Medical Products, Inc. (1993) Summary page 1.

## Most influential descendants
- K230669: L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters (2023), 0 descendants of its own

## Indications for use
The intended use shall be for the administration of fluids, medications, and nutrients; the sampling of blood; and monitoring blood pressure and temperature intravenously. The intended use shall be for the administration of fluids, medications, and nutrients; the sampling of blood; and monitoring blood pressure and temperature intravenously.

Source page: https://510kreport.com/device/K091670
Methodology: https://510kreport.com/methodology