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FDA 510(k)

Vial Adapter 20mm

K-Number: K232875 · 2023-12-14

Decision Date2023-12-14
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vial Adapter 20mm is a medical device manufactured by West Pharma. Services IL, Ltd.. It received FDA 510(k) clearance on 2023-12-14 under approval number K232875. 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 20mm?

Vial Adapter 20mm is a medical device that received FDA 510(k) clearance on 2023-12-14. It is manufactured by West Pharma. Services IL, Ltd.. The 510(k) number is K232875.

When was Vial Adapter 20mm approved by the FDA?

Vial Adapter 20mm received FDA 510(k) clearance on 2023-12-14, under approval number K232875.

What company makes Vial Adapter 20mm?

Vial Adapter 20mm is manufactured by West Pharma. Services IL, Ltd..

What is the FDA product code for Vial Adapter 20mm?

The FDA product code for Vial Adapter 20mm is LHI.

Other Devices by West Pharma. Services IL, Ltd.

Related Devices (Code: LHI)

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.