Vial2Bag Advanced® 20mm Admixture Device
K-Number: K240940 · 2024-05-03
Device Summary
Frequently Asked Questions
What is the Vial2Bag Advanced® 20mm Admixture Device?
Vial2Bag Advanced® 20mm Admixture Device is a medical device that received FDA 510(k) clearance on 2024-05-03. It is manufactured by West Pharmaceutical Services, Inc.. The 510(k) number is K240940.
When was Vial2Bag Advanced® 20mm Admixture Device approved by the FDA?
Vial2Bag Advanced® 20mm Admixture Device received FDA 510(k) clearance on 2024-05-03, under approval number K240940.
What company makes Vial2Bag Advanced® 20mm Admixture Device?
Vial2Bag Advanced® 20mm Admixture Device is manufactured by West Pharmaceutical Services, Inc..
What is the FDA product code for Vial2Bag Advanced® 20mm Admixture Device?
The FDA product code for Vial2Bag Advanced® 20mm Admixture Device is LHI.
Related Clinical Trials
Related PubMed Literature
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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.