# K970763: Modular Telemetry System (MTS) Option for the Mde Escort II Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Medical Data Electronics
- Decided: Jul 14, 1997 after 133 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.
171 later devices descend from it; 4 cite it directly.
0 of 172 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) MDE ESCORT® II+ 400 Series Monitor: named in the summary without a submission number
- (no number) MDE ESCORT® II Series 300 Monitor: named in the summary without a submission number

## Most influential descendants
- K013319: Nonin Model 2120 Pulse Oximeter and Noninvasive Blood Pressure (Nibp) Monitor (2002), 124 descendants of its own
- K041156: Avant Digital Pulse Oximetry System, Models 4000, 4001 (2004), 89 descendants of its own
- K043359: 4100 Patient Oximeter Module (2005), 75 descendants of its own
- K031487: Model Avant 2120 Pulse Oximeter and Nibp (2004), 42 descendants of its own
- K081285: Finger Pulse Oximeter, Model 9560 (2008), 40 descendants of its own

## Indications for use
The MTS Option for the ESCORT II Monitor is a portable monitor intended to be used for monitoring vital signs (ECG & SpO2) of critically ill adult and pediatric patients in the hospital environment.

Source page: https://510kreport.com/device/K970763
Methodology: https://510kreport.com/methodology