# K170965: Fingertip Pulse Oximeter

- Pathway: 510(k) (Special)
- Applicant: Shenzhen Jumper Medical Equipment Co., Ltd.
- Decided: Nov 3, 2017 after 217 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Fingertip Pulse Oximeter (JPD-500F) is non-invasive device intended for spotchecking of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate. The portable fingertip device is indicated for adult and pediatric patients in home and hospital environments (including clinical use in internist/ surgery, anesthesia, intensive care, etc).

Source page: https://510kreport.com/device/K170965
Methodology: https://510kreport.com/methodology