# K053304: Commander Iii Non-Invasive Blood Pressure System

- Pathway: 510(k) (Traditional)
- Applicant: Cardiocom, LLC
- Decided: Dec 30, 2005 after 32 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 K982481 (1998). 1 ancestor in all.
6 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982481: A&D Medical UA-767PC Digital Blood Pressure Monitor, A&D Engineering, Inc. (1998) Summary page 1.

## Most influential descendants
- K122285: Tablet Commander (2012), 5 descendants of its own
- K133252: Healthinterlink Beacon (2014), 3 descendants of its own
- K181248: Comarch e-Care Platform (2018), 2 descendants of its own
- K211822: LifePath Remote Patient Monitoring Platform (2022), 1 descendant of its own
- K252440: EasyTeleMed (2.0.2) (2025), 0 descendants of its own

## Indications for use
The Commander III 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/K053304
Methodology: https://510kreport.com/methodology