AS-3XX Series Fingertip Pulse Oximeter
K-Number: K180685 · 2018-11-29
Device Summary
Frequently Asked Questions
What is the AS-3XX Series Fingertip Pulse Oximeter?
AS-3XX Series Fingertip Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2018-11-29. The listed applicant is Xiamen Acurio Instruments Co., Ltd.. The 510(k) number is K180685.
When did AS-3XX Series Fingertip Pulse Oximeter receive FDA 510(k) clearance?
AS-3XX Series Fingertip Pulse Oximeter received FDA 510(k) clearance on 2018-11-29, under 510(k) number K180685.
Who is the listed applicant for AS-3XX Series Fingertip Pulse Oximeter?
The FDA 510(k) record lists Xiamen Acurio Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AS-3XX Series Fingertip Pulse Oximeter?
The FDA product code for AS-3XX Series 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 Xiamen Acurio Instruments 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.