# K992413: Escort 100/300 Series B (Escort II) Patient Monitor

- Pathway: 510(k) (Special)
- Applicant: Medical Data Electronics
- Decided: Aug 19, 1999 after 30 days
- Product code: DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))
- 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.
27 later devices descend from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) ESCORT® 100/300 Series B (ESCORT II) Patient Monitor (incorporating Nellcor technology): named in the summary without a submission number

## Most influential descendants
- K052446: LG1 Intelligent Medical Vigilance System (2006), 26 descendants of its own
- K082626: PAM 3000 (2009), 21 descendants of its own
- K092062: Everon 1.0 (2010), 10 descendants of its own
- K202464: Vital Sign Monitoring Sensor (Model :XK300) (2021), 9 descendants of its own
- K120465: Earlysense (Everon) System (2012), 9 descendants of its own

## Indications for use
The Medical Data Electronics ESCORT 100/300 Series B Patient Monitor is a portable patient monitor intended to be used for monitoring vital signs of critically ill adult, pediatric and neonatal patients in the hospital environment.

Source page: https://510kreport.com/device/K992413
Methodology: https://510kreport.com/methodology