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FDA 510(k)

Fingertip Pulse Oximeter

K-Number: K181503 · 2018-10-11

Decision Date2018-10-11
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Fingertip Pulse Oximeter is a medical device manufactured by Beijing Choice Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-10-11 under approval number K181503. 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 Fingertip Pulse Oximeter?

Fingertip Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2018-10-11. It is manufactured by Beijing Choice Electronic Technology Co., Ltd.. The 510(k) number is K181503.

When was Fingertip Pulse Oximeter approved by the FDA?

Fingertip Pulse Oximeter received FDA 510(k) clearance on 2018-10-11, under approval number K181503.

What company makes Fingertip Pulse Oximeter?

Fingertip Pulse Oximeter is manufactured by Beijing Choice Electronic Technology Co., Ltd..

What is the FDA product code for Fingertip Pulse Oximeter?

The FDA product code for Fingertip Pulse Oximeter is DQA.

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Official Source

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