# K190026: Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)

- Pathway: 510(k) (Traditional)
- Applicant: Teleflex Medical
- Decided: Aug 21, 2019 after 226 days
- Product code: BSP (Needle, Conduction, Anesthetic (W/Wo Introducer))
- Device class: 2
- Regulation: 21 CFR 868.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K932249 (1993). 13 ancestors in all.
No later device cites it as a predicate yet.
2 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131006: Anesthesia Conduction Needles, Lccs Products Limited (2013) Summary page 4.

## Indications for use
The Arrow Epidural Needles are intended to inject local anesthetic into a patient to provide regional anesthesia or to facilitate the placement of an epidural catheter.

Source page: https://510kreport.com/device/K190026
Methodology: https://510kreport.com/methodology