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. The listed applicant is West Pharmaceutical Services, Inc.. The 510(k) number is K240940.
When did Vial2Bag Advanced® 20mm Admixture Device receive FDA 510(k) clearance?
Vial2Bag Advanced® 20mm Admixture Device received FDA 510(k) clearance on 2024-05-03, under 510(k) number K240940.
Who is the listed applicant for Vial2Bag Advanced® 20mm Admixture Device?
The FDA 510(k) record lists West Pharmaceutical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vial2Bag Advanced® 20mm Admixture Device?
The FDA product code for Vial2Bag Advanced® 20mm Admixture Device is LHI.
Other records listing West Pharmaceutical Services, Inc. as applicant
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.