Pulse Oximeter
K-Number: K201468 · 2021-01-25
Device Summary
Frequently Asked Questions
What is the Pulse Oximeter?
Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2021-01-25. It is manufactured by Shenzhen Creative Industry Co., Ltd.. The 510(k) number is K201468.
When was Pulse Oximeter approved by the FDA?
Pulse Oximeter received FDA 510(k) clearance on 2021-01-25, under approval number K201468.
What company makes Pulse Oximeter?
Pulse Oximeter is manufactured by Shenzhen Creative Industry Co., Ltd..
What is the FDA product code for Pulse Oximeter?
The FDA product code for Pulse Oximeter is DQA.
Related Clinical Trials
Other Devices by Shenzhen Creative Industry 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.