# K101242: Genesis DM Model: 6053000A1

- Pathway: 510(k) (Special)
- Applicant: Honeywell Hommed, LLC
- Decided: Jun 11, 2010 after 39 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: 2 generations back to K040799 (2004). 3 ancestors in all.
18 later devices descend from it; 5 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)
- K061087: Genesis Otc Monitor, Honeywell Hommed, LLC (2006) Summary page 1.
- K061822: Omron Automatic Blood Pressure Monitor with Comfit Cuff, Model Hem 780 N3, Omron Healthcare, Inc. (2006) Summary page 1.

## Most influential descendants
- K112858: Genesis Touch System (2012), 11 descendants of its own
- K122285: Tablet Commander (2012), 5 descendants of its own
- K133252: Healthinterlink Beacon (2014), 3 descendants of its own
- K103214: M3810A Philips Telemonitoring System with Edevice BRIDGED130 (2010), 3 descendants of its own
- K181248: Comarch e-Care Platform (2018), 2 descendants of its own

## Indications for use
The Honeywell HomMed Genesis DM Monitor is designed to retrospectively monitor vital signs. Vital signs include noninvasive blood pressure, pulse rate, and weight. Data from optional commercial stand-alone products extend Genesis DM Monitor's measurement capabilities. Data from the Genesis DM Monitor can be transmitted via a communication module to a central viewing station for display. The Genesis DM Monitor is not intended for emergency use or real-time monitoring.

Source page: https://510kreport.com/device/K101242
Methodology: https://510kreport.com/methodology