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FDA 510(k)

Vial Adapter

K-Number: K232055 · 2023-10-06

ApplicantShanghai Lingfu Technology Co., Ltd.
Decision Date2023-10-06
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vial Adapter is a medical device manufactured by Shanghai Lingfu Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-10-06 under approval number K232055. 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 2023-10-06. It is manufactured by Shanghai Lingfu Technology Co., Ltd.. The 510(k) number is K232055.

When was Vial Adapter approved by the FDA?

Vial Adapter received FDA 510(k) clearance on 2023-10-06, under approval number K232055.

What company makes Vial Adapter?

Vial Adapter is manufactured by Shanghai Lingfu Technology Co., Ltd..

What is the FDA product code for Vial Adapter?

The FDA product code for Vial Adapter is LHI.

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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.

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