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FDA 510(k)

Mecun SpO2 sensor

K-Number: K231979 · 2024-08-16

Decision Date2024-08-16
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Mecun SpO2 sensor is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K231979. 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 Mecun SpO2 sensor?

Mecun SpO2 sensor is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. The 510(k) number is K231979.

When did Mecun SpO2 sensor receive FDA 510(k) clearance?

Mecun SpO2 sensor received FDA 510(k) clearance on 2024-08-16, under 510(k) number K231979.

Who is the listed applicant for Mecun SpO2 sensor?

The FDA 510(k) record lists Shenzhen Mecun Medical Supply Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mecun SpO2 sensor?

The FDA product code for Mecun SpO2 sensor is DQA.

Other records listing Shenzhen Mecun Medical Supply 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

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