# K170047: All-in-One Health Monitor, PC-303

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Creative Industry Co., Ltd.
- Decided: Sep 9, 2017 after 247 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: 12 generations back to K941811 (1994). 118 ancestors in all.
6 later devices descend from it; 3 cite it directly.
1 of 125 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123711: Patient Monitor, Shenzhen Creative Industry Co., Ltd. (2013) Summary page 5.

## Most influential descendants
- K210086: Vitals360 Multi-Vitals Mobile Monitor (2021), 4 descendants of its own
- K212975: MedWand (2022), 1 descendant of its own
- K253436: c-med0 alpha (2026), 0 descendants of its own
- K231116: Multi-parameter detector (2024), 0 descendants of its own
- K231625: VitalDetect (2024), 0 descendants of its own

## Indications for use
The All-in-One Health Monitor PC-303 is a device designed for spot-checking measuring of the patient’s physiological parameters, such as Non-Invasive Blood Pressure (NIBP), Oxygen saturation (SpO2), Pulse Rate (PR) and Body Temperature (TEMP); Additionally, the device is available to communicate with the compatible Blood Glucose Monitoring System and ECG monitor to make the measurement. This device is applicable for Adult and Pediatric (age≥3 years old) use in clinical institutions and has no conditions or factors of contraindication.

Source page: https://510kreport.com/device/K170047
Methodology: https://510kreport.com/methodology