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FDA 510(k)

Vented Vial Adapter Transfer Device - 13mm

K-Number: K160503 · 2016-05-04

ApplicantMedimop Medical Projects, Ltd.
Decision Date2016-05-04
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vented Vial Adapter Transfer Device - 13mm is a medical device manufactured by Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2016-05-04 under approval number K160503. 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 Transfer Device - 13mm?

Vented Vial Adapter Transfer Device - 13mm is a medical device that received FDA 510(k) clearance on 2016-05-04. It is manufactured by Medimop Medical Projects, Ltd.. The 510(k) number is K160503.

When was Vented Vial Adapter Transfer Device - 13mm approved by the FDA?

Vented Vial Adapter Transfer Device - 13mm received FDA 510(k) clearance on 2016-05-04, under approval number K160503.

What company makes Vented Vial Adapter Transfer Device - 13mm?

Vented Vial Adapter Transfer Device - 13mm is manufactured by Medimop Medical Projects, Ltd..

What is the FDA product code for Vented Vial Adapter Transfer Device - 13mm?

The FDA product code for Vented Vial Adapter Transfer Device - 13mm is LHI.

Related Clinical Trials

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Related PubMed Literature

PMID: 41915420 Analysis Model for Infant Incubator Adverse Events Using Retrieval-Augmented Generation Combined With Dual-Adapter Fine-Tuning: Development and Evaluation Study. JMIR medical informatics (2026)

Related Devices (Code: LHI)

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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.

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