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FDA 510(k)

Vent Vial Adapter

K-Number: K233287 · 2024-07-26

ApplicantHangzhou Qiantang Longyue Biotechnology Co., Ltd.
Decision Date2024-07-26
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vent Vial Adapter is a medical device manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2024-07-26 under approval number K233287. 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 Vent Vial Adapter?

Vent Vial Adapter is a medical device that received FDA 510(k) clearance on 2024-07-26. It is manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. The 510(k) number is K233287.

When was Vent Vial Adapter approved by the FDA?

Vent Vial Adapter received FDA 510(k) clearance on 2024-07-26, under approval number K233287.

What company makes Vent Vial Adapter?

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

What is the FDA product code for Vent Vial Adapter?

The FDA product code for Vent Vial Adapter is LHI.

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

K222718Vial 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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