Fingertip Pulse Oximeter
K-Number: K210274 · 2021-07-30
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 2021-07-30. It is manufactured by Zhuhai Linte Medical Instrument Co., Ltd.. The 510(k) number is K210274.
When was Fingertip Pulse Oximeter approved by the FDA?
Fingertip Pulse Oximeter received FDA 510(k) clearance on 2021-07-30, under approval number K210274.
What company makes Fingertip Pulse Oximeter?
Fingertip Pulse Oximeter is manufactured by Zhuhai Linte Medical Instrument 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 Zhuhai Linte Medical Instrument 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.