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FDA 510(k)

WRIST PULSE OXIMETER MD300W

K-Number: K081125 · 2008-07-02

ApplicantBeijing Choice Electronic Technololgy Co., Ltd.
Decision Date2008-07-02
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIST PULSE OXIMETER MD300W is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. It received FDA 510(k) clearance on 2008-07-02 under 510(k) number K081125. 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 WRIST PULSE OXIMETER MD300W?

WRIST PULSE OXIMETER MD300W is a medical device that received FDA 510(k) clearance on 2008-07-02. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K081125.

When did WRIST PULSE OXIMETER MD300W receive FDA 510(k) clearance?

WRIST PULSE OXIMETER MD300W received FDA 510(k) clearance on 2008-07-02, under 510(k) number K081125.

Who is the listed applicant for WRIST PULSE OXIMETER MD300W?

The FDA 510(k) record lists Beijing Choice Electronic Technololgy Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WRIST PULSE OXIMETER MD300W?

The FDA product code for WRIST PULSE OXIMETER MD300W is DQA.

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Other records listing Beijing Choice Electronic Technololgy Co., Ltd. as applicant

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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.

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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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