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FDA 510(k)

Fingertip Pulse Oximeter

K-Number: K210274 · 2021-07-30

Decision Date2021-07-30
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Fingertip Pulse Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Zhuhai Linte Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-07-30 under 510(k) number K210274. 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 2021-07-30. The listed applicant is Zhuhai Linte Medical Instrument Co., Ltd.. The 510(k) number is K210274.

When did Fingertip Pulse Oximeter receive FDA 510(k) clearance?

Fingertip Pulse Oximeter received FDA 510(k) clearance on 2021-07-30, under 510(k) number K210274.

Who is the listed applicant for Fingertip Pulse Oximeter?

The FDA 510(k) record lists Zhuhai Linte Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fingertip Pulse Oximeter?

The FDA product code for Fingertip Pulse Oximeter is DQA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Zhuhai Linte Medical Instrument Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.