# K060820: Cycle BP Monitor and Pulse Oximeter, Model 1060

- Pathway: 510(k) (Abbreviated)
- Applicant: Suntech Medical, Inc.
- Decided: Jun 7, 2006 after 72 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: 7 generations back to K910772 (1991). 22 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053209: Tango+ Automatic Blood Pressure and Oxygen Saturation Measurement System, Suntech Medical, Inc. (2006) Summary page 1.

## Most influential descendants
- K152831: Spot Skan (2016), 0 descendants of its own
- K151512: Star 60 (2016), 0 descendants of its own

## Indications for use
The SunTech Medical Cycle BP monitor and Pulse Oximeter is indicated for use in measuring and displaying systolic and diastolic blood pressures, heart rate, and functional saturation of arterial hemoglobin (SpO2) of adult and pediatric patients in hospitals, medical facilities and subacute environments.

Source page: https://510kreport.com/device/K060820
Methodology: https://510kreport.com/methodology