# K150620: 740 Select

- Pathway: 510(k) (Traditional)
- Applicant: Cas Medical Systems, Inc.
- Decided: May 8, 2015 after 59 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 19 generations back to K941811 (1994). 177 ancestors in all.
No later device cites it as a predicate yet.
1 of 178 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140430: 740 Select, Cas Medical Systems, Inc. (2014) Summary page 4.
- K130740: Nightingale Monitoring System, Zoe Medical, Inc. (2013) Summary page 4.

## Recalls of this device
- Aug 13, 2024 · Class II · Z-3099-2024: This product labeling does not adequately provide warning about the risks associated with the use of damaged batteries or batteries past the intended use life.

## Indications for use
The 740 SELECT series of patient monitors is indicated for use as a portable, multi-parameter, variable acuity device for use by health care professionals, clinicians and medically qualified personnel, in a variety of clinical environments and hospital departments, for non-invasive spot checking, and/or continuous monitoring, recording and alarming of multiple physiological parameters for use in adults, and pediatric patients. The 740 SELECT series monitors come with multiple configurations and optional features. Standard and optional parameters include: • Blood pressure and pulse rate; • Functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate; • Carbon Dioxide concentration of the expired and inspired breath and respiration rate including, with the Covidien Microstream MicroPod option, an Integrated Pulmonary Index (IPI); • Electronic predictive and temporal artery temperature; • ECG and heart rate derived from ECG; • Impedance respiration to detect the rate or absence of respiratory effort with the ECG option for adult, adolescent, child and infant; • Non-invasive monitoring, with Masimo Rainbow SET technology, of carboxyhemoglobin saturation (SpCO) and/or respiration (RRa). Other information displayed includes: Signal IQ Waveform, Low Signal IQ (Low SIQ), Perfusion Index (PI), and/or Pleth Variability Index (PVI) for use during both no motion and motion conditions, and for patients who are well or poorly perfused.

Source page: https://510kreport.com/device/K150620
Methodology: https://510kreport.com/methodology