# K043096: Commander II

- Pathway: 510(k) (Traditional)
- Applicant: Cardiocom
- Decided: Nov 24, 2004 after 15 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K010029 (2001). 1 ancestor in all.
8 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010029: Home Health Monitoring System, Avid Care Corp. (2001) Summary page 1.

## Most influential descendants
- K053303: Cardiocom Commander Iii (2005), 7 descendants of its own
- K091579: Foresee Home (2009), 4 descendants of its own
- K121738: Myvisiontrack (TM) (2013), 3 descendants of its own
- K143211: myVision Track Model 005 (2015), 2 descendants of its own
- K180895: Alleye (2018), 1 descendant of its own

## Indications for use
The Commander II device is for use by patients to collect and transmit general health questions and patient vital sign data (such as weight, blood pressure, glucose, pulse oximetry, peak flow) between the patient, typically at home, and a health care professional at a remote site.

Source page: https://510kreport.com/device/K043096
Methodology: https://510kreport.com/methodology