# K070750: 247 BP Device

- Pathway: 510(k) (Abbreviated)
- Applicant: Suntech Medical, Inc.
- Decided: May 2, 2007 after 44 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: 1 generation back to K002530 (2000). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002530: Welch Allyn Spot Check Device, Welch Allyn, Inc. (2000) Summary page 1.

## Most influential descendants
- K160439: SunTech CT40 Spot-check Vital Signs Device (2016), 1 descendant of its own
- K192092: Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 (2020), 0 descendants of its own

## Indications for use
The SunTech Medical 247 NIBP, Temperature, and Pulse Oximeter device is indicated for use in measuring and displaying Systolic and Diastolic blood pressures, heart rate, temperature, and functional saturation of arterial hemoglobin (Sp02) of adult and pediatric patients in hospitals, medical facilities, clinics, physicians offices, and other subacute environments.

Source page: https://510kreport.com/device/K070750
Methodology: https://510kreport.com/methodology