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FDA 510(k)

Vial Adapter

K-Number: K222718 · 2023-03-10

ApplicantHangzhou Qiantang Longyue Biotechnology Co., Ltd.
Decision Date2023-03-10
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vial Adapter is a medical device manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2023-03-10 under approval number K222718. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vial Adapter?

Vial Adapter is a medical device that received FDA 510(k) clearance on 2023-03-10. It is manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. The 510(k) number is K222718.

When was Vial Adapter approved by the FDA?

Vial Adapter received FDA 510(k) clearance on 2023-03-10, under approval number K222718.

What company makes Vial Adapter?

Vial Adapter is manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd..

What is the FDA product code for Vial Adapter?

The FDA product code for Vial Adapter is LHI.

Other Devices by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.

K233287Vent Vial Adapter K233277Filter Needle for Single Use K233284Vial Adapter with Filter

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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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