# K150266: Remington Medical Inc. Tuohy Epidural Needles

- Pathway: 510(k) (Traditional)
- Applicant: Remington Medical, Inc.
- Decided: Jun 4, 2015 after 120 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: 8 generations back to K840287 (1984). 24 ancestors in all.
No later device cites it as a predicate yet.
3 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990519: Phoenix Epidural & Spinal Needles, Myco Medical Supplies, Inc. (2000) Summary page 4.
- K133632: Perican Ultra, B.Braun Medical, Inc. (2014) Summary page 4.

## Indications for use
Remington Medical, Inc. Tuohy Epidural Needles are to be used to inject local anesthetics into a patient to provide regional anesthesia or to facilitate the placement of an epidural catheter.

Source page: https://510kreport.com/device/K150266
Methodology: https://510kreport.com/methodology