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FDA 510(k)

Vial Adapter

K-Number: K232055 · 2023-10-06

Decision Date2023-10-06
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vial Adapter is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Lingfu Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-10-06 under 510(k) 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. The listed applicant is Shanghai Lingfu Technology Co., Ltd.. The 510(k) number is K232055.

When did Vial Adapter receive FDA 510(k) clearance?

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

Who is the listed applicant for Vial Adapter?

The FDA 510(k) record lists Shanghai Lingfu Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vial Adapter?

The FDA product code for Vial Adapter is LHI.

Related Devices (Code: LHI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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