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FDA 510(k)

LDV((Low Dead Volume )Syringe

K-Number: K220083 · 2022-05-25

Decision Date2022-05-25
Product CodeQNQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LDV((Low Dead Volume )Syringe is a medical device manufactured by Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.. It received FDA 510(k) clearance on 2022-05-25 under approval number K220083. The device is classified under product code QNQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDV((Low Dead Volume )Syringe?

LDV((Low Dead Volume )Syringe is a medical device that received FDA 510(k) clearance on 2022-05-25. It is manufactured by Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.. The 510(k) number is K220083.

When was LDV((Low Dead Volume )Syringe approved by the FDA?

LDV((Low Dead Volume )Syringe received FDA 510(k) clearance on 2022-05-25, under approval number K220083.

What company makes LDV((Low Dead Volume )Syringe?

LDV((Low Dead Volume )Syringe is manufactured by Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd..

What is the FDA product code for LDV((Low Dead Volume )Syringe?

The FDA product code for LDV((Low Dead Volume )Syringe is QNQ.

Other Devices by Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.

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Related Devices (Code: QNQ)

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.