# K063087: Modification to Model 750 Series Monitor

- Pathway: 510(k) (Special)
- Applicant: Cas Medical Systems, Inc.
- Decided: Dec 11, 2006 after 62 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- 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
Longest line of descent: 9 generations back to K962603 (1997). 31 ancestors in all.
No later device cites it as a predicate yet.
1 of 32 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051896: Model 750E Series Monitor, Cas Medical Systems, Inc. (2005)

## Indications for use
The 750E Patient Monitor is intended to continuously monitor a patients ECG, heart rate, non-invasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), respiration rate, temperature and end tidal carbon dioxide (C02). The monitor is designed as a bedside/portable monitor and is intended for use on adult, pediatric and neonatal patients in the care of health care professionals.

Source page: https://510kreport.com/device/K063087
Methodology: https://510kreport.com/methodology