# K182960: ReliefBand

- Pathway: 510(k) (Special)
- Applicant: Reliefband Technologies, LLC
- Decided: Jun 21, 2019 after 239 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 K173233 (2017). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173233: ReliefBand 1.5, Reliefband Technologies (2017) Summary page 4.

## Most influential descendants
- K191547: ReliefBand (2019), 0 descendants of its own

## Indications for use
ReliefBand 2.0 is indicated for use in the treatment of nausea, retching and vomiting due to motion sickness, chemotherapy and morning sickness associated with pregnancy. ReliefBand 2.0 is also indicated as an adjunct to antiemetics in reducing postoperative nausea.

Source page: https://510kreport.com/device/K182960
Methodology: https://510kreport.com/methodology