# K082280: Suresigns VS2 Vital Signs Monitor, Suresigns VM1 Patient Monitor, Suresigns VS3 Cital Signs Monitor

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems North America Co.
- Decided: Oct 8, 2008 after 58 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K941811 (1994). 24 ancestors in all.
11 later devices descend from it; 4 cite it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052707: M3046B Compact Portable Patient Monitors, Philips Medical Systems (2005) Summary page 1.
- K080495: Suresigns VM Series Patient Monitor, Models VM4, VM6, VM8, VM3 and VS3, Philips Medical Systems (2008) Summary page 1.

## Most influential descendants
- K120132: Suresigns VS3 Vital Signs Monitor, Suresigns VS4 Vital Signs Monitor (2012), 6 descendants of its own
- K133961: Suresigns VS3, Suresigns VS4 (2014), 3 descendants of its own
- K151761: SureSigns VS3, SureSigns VS4 (2015), 2 descendants of its own
- K163649: SureSigns VS3; SureSigns VS4 (2017), 1 descendant of its own
- K110803: Suresigns Vsi Vital Signs Monitor (2011), 1 descendant 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.

Source page: https://510kreport.com/device/K082280
Methodology: https://510kreport.com/methodology