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FDA 510(k)

Pulse Oximeter

K-Number: K201468 · 2021-01-25

Decision Date2021-01-25
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Pulse Oximeter is a medical device manufactured by Shenzhen Creative Industry Co., Ltd.. It received FDA 510(k) clearance on 2021-01-25 under approval number K201468. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.