# K963271: Futrex-6100/XL

- Pathway: 510(k) (Traditional)
- Applicant: Futrex, Inc.
- Decided: Aug 19, 1998 after 729 days
- Product code: MNW (Analyzer, Body Composition)
- Device class: 2
- Regulation: 21 CFR 870.2770
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K143108: HealthGuard-15 (2015), 0 descendants of its own
- K033452: CWAS 1000 (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K963271
Methodology: https://510kreport.com/methodology