# K113662: Fenestrated Nerve Block Needle

- Pathway: 510(k) (Traditional)
- Applicant: Imd, Inc.
- Decided: Apr 20, 2012 after 135 days
- Product code: CAZ (Anesthesia Conduction Kit)
- Device class: 2
- Regulation: 21 CFR 868.5140
- 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). 14 ancestors in all.
No later device cites it as a predicate yet.
2 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052946: MPS Acacia Nerve Block Needle, Mps Acacia (2005) Summary page 1.
- K073187: Peripheral Nerve Block Support Tray, Life-Tech, Inc. (2008) Summary page 1.

## Indications for use
IMD's New Fenestrated Nerve Block Needle is a single patient use needle to provide local or regional nerve blocking by the injecting of a local anesthesia. It is to be used only under the direction of a licensed clinician.

Source page: https://510kreport.com/device/K113662
Methodology: https://510kreport.com/methodology