# K925529: Wander Care

- Pathway: 510(k) (Traditional)
- Applicant: Care Electronics, Inc.
- Decided: Jun 16, 1993 after 226 days
- Product code: KMI (Monitor, Bed Patient)
- Device class: 1
- Regulation: 21 CFR 880.2400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 1 cites it directly.
0 of 16 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
- K090138: Mobilecare Monitor, Model 2100 (2009), 14 descendants of its own
- K101109: Vivatrak (2010), 12 descendants of its own
- K130752: Dynasense System (2013), 6 descendants of its own
- K141877: Leaf Patient Monitoring System (2014), 5 descendants of its own
- K191882: Masimo Centroid System (2020), 3 descendants of its own

Source page: https://510kreport.com/device/K925529
Methodology: https://510kreport.com/methodology