# K132038: Accutorr 7 Vital Signs Monitor

- Pathway: 510(k) (Abbreviated)
- Applicant: Mindray North America
- Decided: May 2, 2014 after 305 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 K933143 (1994). 45 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 48 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072235: PM-50 Pulse Oximeter and VS-800 Vital Signs Monitor, Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (2007) Summary page 1.

## Most influential descendants
- K170712: Accutorr 7/VS-900 Vital Signs Monitor (2017), 1 descendant of its own
- K182821: Accutorr 7/VS-900/VS-900c Vital Signs Monitor (2019), 0 descendants of its own

## Indications for use
The Accutorr 7 Vital Signs Monitor is intended for monitoring physiologic parameters, including SpO2. PR, NISP and TEMP, on adult, pediatric, and neonatal patients in healthcare facilities by clinical physicians or appropriate medical staff under the direction of physicians

Source page: https://510kreport.com/device/K132038
Methodology: https://510kreport.com/methodology