# K092970: General Patient Monitors, Models: G3C/ G3D/ G3F/ G3G/ G3H

- Pathway: 510(k) (Traditional)
- Applicant: General Meditech, Inc.
- Decided: Feb 2, 2010 after 130 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K941811 (1994). 90 ancestors in all.
No later device cites it as a predicate yet.
0 of 91 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072346: PM-7000 Patient Monitor, Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (2007) Summary page 1.

## Indications for use
General Patient Monitors is intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters including ECG Heart Rate (HR), Respiration Rate (RESP), Pulse Oxygen Saturation (SpO2),. Pulse Rate (PR), Non-invasive Blood Pressure (NIBP), Invasive Blood Pressure (11BP), carbon dioxide (C02), and Temperature (TEMP) of adult, pediatric and neonatal patient. The monitor is to be used in healthcare facilities by clinical physicians or appropriate medical staff under the direction of physicians. It is not intended for helicopter transport or hospital ambulance.

Source page: https://510kreport.com/device/K092970
Methodology: https://510kreport.com/methodology