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FDA 510(k)

Fingertip Pulse Oximeter MD300CN310

K-Number: K161560 · 2016-10-05

ApplicantBeijing Choice Electronic Technology Co., Ltd.
Decision Date2016-10-05
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Fingertip Pulse Oximeter MD300CN310 is a medical device manufactured by Beijing Choice Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2016-10-05 under approval number K161560. 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 MD300CN310?

Fingertip Pulse Oximeter MD300CN310 is a medical device that received FDA 510(k) clearance on 2016-10-05. It is manufactured by Beijing Choice Electronic Technology Co., Ltd.. The 510(k) number is K161560.

When was Fingertip Pulse Oximeter MD300CN310 approved by the FDA?

Fingertip Pulse Oximeter MD300CN310 received FDA 510(k) clearance on 2016-10-05, under approval number K161560.

What company makes Fingertip Pulse Oximeter MD300CN310?

Fingertip Pulse Oximeter MD300CN310 is manufactured by Beijing Choice Electronic Technology Co., Ltd..

What is the FDA product code for Fingertip Pulse Oximeter MD300CN310?

The FDA product code for Fingertip Pulse Oximeter MD300CN310 is DQA.

Related Clinical Trials

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Other Devices by Beijing Choice Electronic Technology Co., Ltd.

K160268Fingertip Pulse Oximeter MD300CG11/MD300CG51 K152563Pulse Oximeter (MD300M/MD300K2) K162089Blood Pressure Monitor K181503Fingertip Pulse Oximeter K172366Wrist Pulse Oximeter K211754Vital Signs Monitor

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Related Devices (Code: DQA)

K162675Masimo Rainbow SET Intellivue Module Pulse CO-OximeterMasimo Corporation K160231Model X-100C CO-Met™ Oximetry SystemNonin Medical, Inc. K160940Masimo Disposable Transflectance Forehead SensorMasimo Corporation K153021Fingertip Pulse Oximeter A310Amemo, Inc. K160268Fingertip Pulse Oximeter MD300CG11/MD300CG51Beijing Choice Electronic Technology Co., Ltd. K160582WiCapAthena Gtx

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.

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