# K202497: Aulisa Multiple Patient Digital Vital Sign Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Taiwan Aulisa Medical Devices Technologies, Inc.
- Decided: Oct 30, 2020 after 60 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- 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: 7 generations back to K925411 (1993). 15 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151006: EarlySense Central Display Station (CDS), Earlysense, Ltd. (2015) Summary page 4.

## Most influential descendants
- K242842: ANNE View, Central Hub (2025), 1 descendant of its own
- K243837: iBSM (2025), 0 descendants of its own

## Indications for use
The Aulisa Multiple Patient Digital Vital Sign Monitoring System, MP1000, is intended to provide remote central monitoring and display of information as recorded by multiple Aulisa single-patient monitoring systems, on a central remote screen. The system can be used in a hospital type and clinic environment.

Source page: https://510kreport.com/device/K202497
Methodology: https://510kreport.com/methodology