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FDA 510(k)

HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M

K-Number: K100203 · 2010-05-17

ApplicantBeijing Choice Electronic Technololgy Co., Ltd.
Decision Date2010-05-17
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M 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 2010-05-17 under 510(k) number K100203. 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 HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M?

HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M is a medical device that received FDA 510(k) clearance on 2010-05-17. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K100203.

When did HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M receive FDA 510(k) clearance?

HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M received FDA 510(k) clearance on 2010-05-17, under 510(k) number K100203.

Who is the listed applicant for HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M?

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 HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M?

The FDA product code for HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M 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)

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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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