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FDA 510(k)

NEXUS I.V. FLUID TRANSFER DEVICE

K-Number: K080976 · 2008-11-10

ApplicantNexus Medical, LLC
Decision Date2008-11-10
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEXUS I.V. FLUID TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Nexus Medical, LLC. It received FDA 510(k) clearance on 2008-11-10 under 510(k) number K080976. 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 NEXUS I.V. FLUID TRANSFER DEVICE?

NEXUS I.V. FLUID TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 2008-11-10. The listed applicant is Nexus Medical, LLC. The 510(k) number is K080976.

When did NEXUS I.V. FLUID TRANSFER DEVICE receive FDA 510(k) clearance?

NEXUS I.V. FLUID TRANSFER DEVICE received FDA 510(k) clearance on 2008-11-10, under 510(k) number K080976.

Who is the listed applicant for NEXUS I.V. FLUID TRANSFER DEVICE?

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

What is the FDA product code for NEXUS I.V. FLUID TRANSFER DEVICE?

The FDA product code for NEXUS I.V. FLUID TRANSFER DEVICE is LHI.

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Other records listing Nexus Medical, LLC 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.

K130879NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUSK130416NEXUS TKO-6P LUER ACTIVATED DEVICEK113398NEXUS TKO-6, LUER-ACTIVATED DEVICEK092382NEXUS PRESSURE RATED EXTENSION SETSK092930NEXUS INTRAVASCULAR TUBING SETS-PRE-PIERCEDK092527NEXUS INJECTION SITE, MODEL NIS-8

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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.

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