Fingertip Pulse Oximeter
K-Number: K170965 · 2017-11-03
Device Summary
Frequently Asked Questions
What is the Fingertip Pulse Oximeter?
Fingertip Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2017-11-03. It is manufactured by Shenzhen Jumper Medical Equipment Co., Ltd.. The 510(k) number is K170965.
When was Fingertip Pulse Oximeter approved by the FDA?
Fingertip Pulse Oximeter received FDA 510(k) clearance on 2017-11-03, under approval number K170965.
What company makes Fingertip Pulse Oximeter?
Fingertip Pulse Oximeter is manufactured by Shenzhen Jumper Medical Equipment Co., Ltd..
What is the FDA product code for Fingertip Pulse Oximeter?
The FDA product code for Fingertip Pulse Oximeter is DQA.
Related Clinical Trials
Other Devices by Shenzhen Jumper Medical Equipment Co., Ltd.
Related Devices (Code: DQA)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.