# K014025: Hommed Sentry Iii Patient Monitor System with Card Reader

- Pathway: 510(k) (Traditional)
- Applicant: Hommed, LLC
- Decided: Apr 9, 2002 after 124 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
21 later devices descend from it; 2 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) HomMed Sentry III Patient Monitor System: named in the summary without a submission number

## Most influential descendants
- K030797: S7 Elite Cpap System with Somnotraxx System; Autoset Spirit Cpap System with Somnotraxx System (2004), 17 descendants of its own
- K051314: Res Traxx Data Center (2005), 16 descendants of its own
- K053205: Res Traxx Data Center (2006), 15 descendants of its own
- K070746: Restraxx Data Centre, Model R10 (2007), 14 descendants of its own
- K083816: Res Traxx Online, Model: R14 (2009), 13 descendants of its own

## Indications for use
The HomMed Sentry III Patient Monitor System with Card Reader is designed to measure Patient Vital Signs in the home by patients or in clinical environments by health care providers. The HomMed Sentry III Patient Monitor System with Card Reader is available with physicians’ orders only. The HomMed Sentry III Patient Monitor System with Card Reader allows patients to use multiple Sentry III monitors or multiple patients to use the same Sentry III monitor. The HomMed Sentry III Patient Monitor System with Card Reader measures the following parameters: Non-Invasive Blood Pressures (Systolic, Diastolic and Mean Arterial Pressure), Functional Oxygen Saturation (%SpO2), Peripheral Pulse Rate (PPR), Pulse Strength, Oral Temperature and Patient Weight via an external scale. The HomMed Sentry III Patient Monitor System with Card Reader’s optional, compatible devices extends those measurements to glucometer and spirometer monitoring. The patient parameter data is collected and displayed by the HomMed Sentry III Patient Monitor System with Card Reader. Data can be transmitted via the communication module to a central station where the patient data can be viewed and analyzed.

Source page: https://510kreport.com/device/K014025
Methodology: https://510kreport.com/methodology