# K002835: Bodystat

- Pathway: 510(k) (Traditional)
- Applicant: Bodystat, Ltd.
- Decided: Jul 3, 2001 after 294 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.
34 later devices descend from it; 8 cite it directly.
0 of 35 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
- K050415: Impedimed-Extracellular Fluid Analysis (2007), 11 descendants of its own
- K023478: Inbody AP1 Body Composition Analyzer (2003), 11 descendants of its own
- K080825: Impedimed Extra Cellular Fluid Analysis, Model L-Dex U400 (2008), 10 descendants of its own
- K042528: Inbody, Model 3.0 (2005), 10 descendants of its own
- K052646: Biospace Body Composition Analyzers, Models Inbody 520, 720 and S20 (2005), 8 descendants of its own

Source page: https://510kreport.com/device/K002835
Methodology: https://510kreport.com/methodology