# K110803: Suresigns Vsi Vital Signs Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems
- Decided: May 20, 2011 after 58 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K941811 (1994). 26 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082280: Suresigns VS2 Vital Signs Monitor, Suresigns VM1 Patient Monitor, Suresigns VS3 Cital Signs Monitor, Philips Medical Systems North America Co. (2008) Summary page 1.
- K090483: Sursigns VS2 Vital Signs Monitor, Suresigns VS3 Vital Signs Monitor, Suresigns VM Series Patient Monitors, Philips Medical Systems (2009) Summary page 1.

## Most influential descendants
- K112652: Suresigns VS2+ -Suresigns Vsi (2011), 0 descendants of its own

## Indications for use
Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Standard and optional parameters include: NBP SP02 Temperature

Source page: https://510kreport.com/device/K110803
Methodology: https://510kreport.com/methodology