# K120193: Any View Patient Monitors

- Pathway: 510(k) (Traditional)
- Applicant: Guangdong Biolight Meditech Co., Ltd.
- Decided: Jun 29, 2012 after 158 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
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K131898: A Series and Q Series Patient Monitors (2014), 2 descendants of its own
- K183687: LifeWindow LW8 Lite (2019), 1 descendant of its own
- K200434: V20, V20a, AVSM3 SNF (2020), 0 descendants of its own
- K131763: Truscope Series Patient Monitor (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K120193
Methodology: https://510kreport.com/methodology