Vented Vial Adapter 20mm
K-Number: K213513 · 2022-08-31
ApplicantWest Pharma. Services IL, Ltd.
Decision Date2022-08-31
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Vented Vial Adapter 20mm is a medical device manufactured by West Pharma. Services IL, Ltd.. It received FDA 510(k) clearance on 2022-08-31 under approval number K213513. 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 Vented Vial Adapter 20mm?
Vented Vial Adapter 20mm is a medical device that received FDA 510(k) clearance on 2022-08-31. It is manufactured by West Pharma. Services IL, Ltd.. The 510(k) number is K213513.
When was Vented Vial Adapter 20mm approved by the FDA?
Vented Vial Adapter 20mm received FDA 510(k) clearance on 2022-08-31, under approval number K213513.
What company makes Vented Vial Adapter 20mm?
Vented Vial Adapter 20mm is manufactured by West Pharma. Services IL, Ltd..
What is the FDA product code for Vented Vial Adapter 20mm?
The FDA product code for Vented Vial Adapter 20mm is LHI.
Other Devices by West Pharma. Services IL, Ltd.
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.