# K173233: ReliefBand 1.5

- Pathway: 510(k) (Traditional)
- Applicant: Reliefband Technologies
- Decided: Nov 30, 2017 after 56 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.
2 later devices descend from it; 2 cite 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)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K182960: ReliefBand (2019), 1 descendant of its own
- K191547: ReliefBand (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K173233
Methodology: https://510kreport.com/methodology