# K992411: Escort II+ 400 Series (Escort Prism) Monitor

- Pathway: 510(k) (Special)
- Applicant: Medical Data Electronics
- Decided: Aug 18, 1999 after 29 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.
No later device cites it as a predicate yet.
0 of 1 device 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

## 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/K992411
Methodology: https://510kreport.com/methodology