# K014294: Modification to Escort II+ 400 Series 9ESCORT Prism) Monitor, Models 20400, 20401, 20403, 20411, 20412, 20413, 20414

- Pathway: 510(k) (Special)
- Applicant: Medical Data Electronics
- Decided: Jan 25, 2002 after 28 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
0 of 13 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 II+ 400 Series (ESCORT Prism) Monitor: named in the summary without a submission number

## Most influential descendants
- K062144: Escort M8 Vital Signs Patient Monitor, Model 3810 (2006), 11 descendants of its own
- 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

## Indications for use
The Medical Data Electronics ESCORT II+ 400 Series 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/K014294
Methodology: https://510kreport.com/methodology