# K062144: Escort M8 Vital Signs Patient Monitor, Model 3810

- Pathway: 510(k) (Traditional)
- Applicant: Invivo Corporation
- Decided: Oct 12, 2006 after 77 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: 5 generations back to K933143 (1994). 37 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001775: Zoe Medical Nightingale Monitoring System, Zoe Medical, Inc. (2001)
- K014294: Modification to Escort II+ 400 Series 9ESCORT Prism) Monitor, Models 20400, 20401, 20403, 20411, 20412, 20413, 20414, Medical Data Electronics (2002) Summary page 2.
- K040011: Polaris 2004 Capnograph, Oridion, Ltd. (2004) Summary page 2.
- K992340: Masimo Set Radical Pulse Oximeter with Satshare, Masimo Lnop -Adt-Adult/Pediatric Disposable Sensor, Masimo Lnop -PDT-PE, Masimo Corp. (1999) Summary page 2.
- K020550: Passport 2 with View 12 Ecg Analysis Module Model # 0998-00-0170-XXXX, Datascope Corp. (2002) Summary page 2.

## Most influential descendants
- K090556: Spacelabs Elance Vital Signs Monitoring System and Central Monitor Software (2009), 10 descendants of its own
- K130740: Nightingale Monitoring System (2013), 3 descendants of its own
- K123556: Mortara Surveyor Patient Monitor (2013), 2 descendants of its own
- K161517: Mortara Surveyor Patient Monitor (2017), 1 descendant of its own
- K152043: Diagnostic Station DS20 (2016), 1 descendant of its own

## Indications for use
The Escort M8 Vital Signs Patient Monitor Model 3810 is intended for use as a vital signs monitor for adult and pediatric patients in a hospital setting.

Source page: https://510kreport.com/device/K062144
Methodology: https://510kreport.com/methodology