Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Vial Adapter 20mm

K-Number: K232875 · 2023-12-14

Decision Date2023-12-14
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vial Adapter 20mm is the device name listed in this FDA 510(k) record. The listed applicant is West Pharma. Services IL, Ltd.. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K232875. 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 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.