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)

Arisure Closed Vial Adapter

K-Number: K172884 · 2017-10-03

ApplicantYukon Medical
Decision Date2017-10-03
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Arisure Closed Vial Adapter is the device name listed in this FDA 510(k) record. The listed applicant is Yukon Medical. It received FDA 510(k) clearance on 2017-10-03 under 510(k) number K172884. 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 Arisure Closed Vial Adapter?

Arisure Closed Vial Adapter is a medical device that received FDA 510(k) clearance on 2017-10-03. The listed applicant is Yukon Medical. The 510(k) number is K172884.

When did Arisure Closed Vial Adapter receive FDA 510(k) clearance?

Arisure Closed Vial Adapter received FDA 510(k) clearance on 2017-10-03, under 510(k) number K172884.

Who is the listed applicant for Arisure Closed Vial Adapter?

The FDA 510(k) record lists Yukon Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arisure Closed Vial Adapter?

The FDA product code for Arisure Closed Vial Adapter is LHI.

Other records listing Yukon Medical 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.

K240761Arisure® Closed Male Luer with Spike Adapter (YM060)K243486SmartSiteTM Vented Vial Access DeviceK201422Arisure Closed System Drug Transfer Device (CSTD)K172631Arisure Dry SpikeK171101Closed Male Luer

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.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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.

↑