# K924234: Cons. Current Periph. Nerve Loc. NS232,NS262,NS272

- Pathway: 510(k) (Traditional)
- Applicant: Fisher & Paykel Electronics, Ltd.
- Decided: May 27, 1993 after 276 days
- Product code: KOI (Stimulator, Nerve, Peripheral, Electric)
- Device class: 2
- Regulation: 21 CFR 868.2775
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K953205: Constant Current Peripheral Nerve Stimulator NS272 (Modification) (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K924234
Methodology: https://510kreport.com/methodology