# K131006: Anesthesia Conduction Needles

- Pathway: 510(k) (Traditional)
- Applicant: Lccs Products Limited
- Decided: Dec 6, 2013 after 239 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: 4 generations back to K932249 (1993). 12 ancestors in all.
5 later devices descend from it; 2 cite it directly.
2 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070354: Imd's Anesthesia Needles (Tuohy, Quincke and Pencil Point), International Medical Development, Inc. (2007) Summary page 1.

## Most influential descendants
- K142553: UNIEVER Disposable Epidural Anesthesia Needle, UNIEVER Disposable Nerve Blocked Needle (2015), 3 descendants of its own
- K171518: Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles (2018), 2 descendants of its own
- K212982: Medispine - Spinal Needle, Glospine - Spinal Needle (2022), 0 descendants of its own
- K211085: BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle (2022), 0 descendants of its own
- K190026: Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) (2019), 0 descendants of its own

## Indications for use
AN-E epidural needle is intended for the transient delivery of anesthetics to provide neuraxial anesthesia or to facilitate placement of an epidural catheter.

Source page: https://510kreport.com/device/K131006
Methodology: https://510kreport.com/methodology