# K173300: ViaTherm BOOST

- Pathway: 510(k) (Traditional)
- Applicant: Viatherm Therapeutics, LLC
- Decided: May 1, 2018 after 196 days
- Product code: IMJ (Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5290
- 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
- K250376: ViVY (2025), 0 descendants of its own
- K223620: Reprieve by RegenesisTM (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K173300
Methodology: https://510kreport.com/methodology