Vial Adapter 20mm
K-Number: K232875 · 2023-12-14
Device Summary
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. The listed applicant is West Pharma. Services IL, Ltd.. The 510(k) number is K232875.
When did Vial Adapter 20mm receive FDA 510(k) clearance?
Vial Adapter 20mm received FDA 510(k) clearance on 2023-12-14, under 510(k) number K232875.
Who is the listed applicant for Vial Adapter 20mm?
The FDA 510(k) record lists West Pharma. Services IL, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vial Adapter 20mm?
The FDA product code for Vial Adapter 20mm is LHI.
Other records listing West Pharma. Services IL, Ltd. 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.