# K122690: Ultraquik Peripheral Nerve Block Needle

- Pathway: 510(k) (Traditional)
- Applicant: Arrow International, Inc.
- Decided: Dec 21, 2012 after 108 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: 1 generation back to K014246 (2002). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014246: Avid-Nit Nerve Stimulation Needles, Avid N.I.T., Inc. (2002) Summary page 2.

## Indications for use
The Arrow UltraQuik® Peripheral Nerve Block Needle is indicated for the delivery of single-shot peripheral nerve block anesthesia or analgesia using medical imaging devices.

Source page: https://510kreport.com/device/K122690
Methodology: https://510kreport.com/methodology