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FDA 510(k)

Mix2Vial® Transfer Device

K-Number: K231071 · 2024-01-19

ApplicantWest Pharma. Services IL, Ltd.
Decision Date2024-01-19
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Mix2Vial® Transfer Device is a medical device manufactured by West Pharma. Services IL, Ltd.. It received FDA 510(k) clearance on 2024-01-19 under approval number K231071. 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 Mix2Vial® Transfer Device?

Mix2Vial® Transfer Device is a medical device that received FDA 510(k) clearance on 2024-01-19. It is manufactured by West Pharma. Services IL, Ltd.. The 510(k) number is K231071.

When was Mix2Vial® Transfer Device approved by the FDA?

Mix2Vial® Transfer Device received FDA 510(k) clearance on 2024-01-19, under approval number K231071.

What company makes Mix2Vial® Transfer Device?

Mix2Vial® Transfer Device is manufactured by West Pharma. Services IL, Ltd..

What is the FDA product code for Mix2Vial® Transfer Device?

The FDA product code for Mix2Vial® Transfer Device is LHI.

Related Clinical Trials

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Other Devices by West Pharma. Services IL, Ltd.

K213513Vented Vial Adapter 20mm K232875Vial Adapter 20mm K230988Vial2Bag Advanced® 13mm Admixture Device K230464MixJect® Transfer Device

Related Devices (Code: LHI)

K161800OnSite-IVPharmc, LLC K160503Vented Vial Adapter Transfer Device - 13mmMedimop Medical Projects, Ltd. K151423APEX Compounding System Transfer SetB.Braun Medical, Inc. K162216GRI-FILL PERISTALTIC SETLaboratorios Grifols, S.A. K171796Vial Adapter 15mmMedimop Medical Project , Ltd. K172884Arisure Closed Vial AdapterYukon Medical

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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