# K982967: Reliefband MST Device, Models RB-2, RB-6, RB-R

- Pathway: 510(k) (Traditional)
- Applicant: Woodside Biomedical, Inc.
- Decided: Feb 23, 1999 after 182 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
No predicates in its family tree.
18 later devices descend from it; 2 cite it directly.
0 of 19 devices 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.

## Most influential descendants
- K020180: Reliefband Device, Models RB-DL, RB-EL, RB-RL (2002), 17 descendants of its own
- K033268: Sea-Band (2004), 10 descendants of its own
- K041877: Acu-Strap Motion Sickness Band (2004), 7 descendants of its own
- K110563: Pressure Right, Single-Use, Disposable, Pressure-Sensitive Emetic-Management Wrist Strip (2011), 4 descendants of its own
- K142471: Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist Strip (2014), 3 descendants of its own

## Indications for use
The ReliefBand® Device is indicated for the relief of nausea and vomiting (NV) due to motion sickness

Source page: https://510kreport.com/device/K982967
Methodology: https://510kreport.com/methodology