# K040651: Hommed Sentry Iiib-F Patient Monitor System

- Pathway: 510(k) (Traditional)
- Applicant: Hommed, LLC
- Decided: Aug 10, 2004 after 152 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 K014025 (2002). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014025: Hommed Sentry Iii Patient Monitor System with Card Reader, Hommed, LLC (2002) Summary page 1.

## Most influential descendants
- K061088: Sentry Otc Monitor (2006), 0 descendants of its own
- K050951: Medstar 220, Model 533-220; Medstar 230, Model 533-230; Medstar 360, Model 533-360; Medstar 370, Model 533-370 (2005), 0 descendants of its own

## Indications for use
The HomMed Sentry 111B-F Patient Monitor System is designed to measure Patient Vital Signs in the home by patients or in clinical environments by health care providers. The HomMed Sentry 111B-F Patient Monitor System is available with physicians' orders only. The HomMed Sentry IllB-F Patient Monitor System measures the following parameters: Non-Invasive Blood Pressures (Systolic, Diastolic and Mean Arterial Pressure), Functional Oxygen Saturation (%SP 0 2), Peripheral Pulse Rate (PPR), Pulse Strength, Oral Temperature and Patient Weight via an external scale. The HomMed Sentry 111B-F Patient Monitor System's optional, compatible devices extend those measurements to glucometer, spirometer, electrocardiogram (ECG) and prothrombin time (PT/INR) monitoring and digital image acquisition. The patient parameter data is collected and displayed by the HomMed Sentry 111B-F Patient Monitor System. 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/K040651
Methodology: https://510kreport.com/methodology