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FDA 510(k)

Denudation Pipettes

K-Number: K250838 · 2025-07-03

ApplicantGuangzhou Pinzhi Medical Device Co., Ltd.
Decision Date2025-07-03
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Denudation Pipettes is a medical device manufactured by Guangzhou Pinzhi Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2025-07-03 under approval number K250838. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Denudation Pipettes?

Denudation Pipettes is a medical device that received FDA 510(k) clearance on 2025-07-03. It is manufactured by Guangzhou Pinzhi Medical Device Co., Ltd.. The 510(k) number is K250838.

When was Denudation Pipettes approved by the FDA?

Denudation Pipettes received FDA 510(k) clearance on 2025-07-03, under approval number K250838.

What company makes Denudation Pipettes?

Denudation Pipettes is manufactured by Guangzhou Pinzhi Medical Device Co., Ltd..

What is the FDA product code for Denudation Pipettes?

The FDA product code for Denudation Pipettes is MQH.

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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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