# K133252: Healthinterlink Beacon

- Pathway: 510(k) (Traditional)
- Applicant: Healthinterlink, LLC
- Decided: Mar 14, 2014 after 143 days
- Product code: DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 870.2910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K864318 (1987). 71 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 75 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112559: Medapps 2.0 Remote Patient Monitoring System, Medapps, Inc. (2011)
- K112858: Genesis Touch System, Honeywell Hommed, LLC (2012)
- K122285: Tablet Commander, Cardiocom, LLC (2012) Summary page 1.
- K103276: Intel Health Guide, Intel Corporation Digital Health Group (2011) Summary page 1.

## Most influential descendants
- 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 HealthInterlink® Beacon® device is for use by patients to collect and transmit general health information, physiological measurements such as blood pressure, temperature, weight, glucose and SpO2 using commercially available FDA cleared wireless medical devices designed for home use, and other data between themselves and a caregiver. The HealthInterlink® Beacon® makes no diagnosis. Clinical judgment and experience are required to check and interpret the information transmitted. HealthInterlink® Beacon® is not intended as a substitute for medical care.

Source page: https://510kreport.com/device/K133252
Methodology: https://510kreport.com/methodology