# K032196: NBD Disposable RF Cannulae

- Pathway: 510(k) (Traditional)
- Applicant: New Business Development, LLC
- Decided: Oct 9, 2003 after 83 days
- Product code: GXI (Probe, Radiofrequency Lesion)
- Device class: 2
- Regulation: 21 CFR 882.4725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The NBD Disposable RF Needle are indicated for use in radio frequency heat lesion procedures for relief of pain.

Source page: https://510kreport.com/device/K032196
Methodology: https://510kreport.com/methodology