# K172221: VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100

- Pathway: 510(k) (Traditional)
- Applicant: Taidoc Technology Corporation
- Decided: Jun 6, 2018 after 317 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K982481 (1998). 29 ancestors in all.
No later device cites it as a predicate yet.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101259: V-Trust TD-8002 Multi-Parameter Spot-Check Monitor Model TD-8002, Taidoc Technology Corporation (2010) Summary page 5.
- K101569: V-Trust Model TD-2202 Portable Ecg Recorder, Taidoc Technology Corporation (2011) Summary page 5.
- K120042: TD-4268 Blood Glucose Monitoring System TD-4268 Multi Blood Glucose Monitoring System, Taidoc Technology Corporation (2012) Summary page 5.

## Indications for use
The Vital Signs Monitor is intended for the monitoring of parameters such as ECG, non-invasive blood pressure (systolic, diastolic, and mean arterial pressure), pulse rate, body temperature, blood glucose and oxygen saturation of arterial hemoglobin (SpO2) of adult patient. The monitor is intended to be used by clinicians and medically qualified personnel and trained users.

Source page: https://510kreport.com/device/K172221
Methodology: https://510kreport.com/methodology