# K123958: Jiajian Pointoselect Digital

- Pathway: 510(k) (Traditional)
- Applicant: Wuxi Jiajian Medical Instrument Co., Ltd.
- Decided: Oct 28, 2013 after 311 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- Device class: 2
- Regulation: 21 CFR 882.5890
- 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 K060517 (2006). 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)
- K060517: Pointer Excel, Lhasa Oms, Inc. (2006) Summary page 4.

## Indications for use
The Jiajian® Pointoselect Digital is intended for use in the symptomatic relief of chronic intractable pain, postoperative pain, and acute pain.

Source page: https://510kreport.com/device/K123958
Methodology: https://510kreport.com/methodology