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