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FDA 510(k)

MIX2VIAL TRANSFER DEVICE

K-Number: K031861 · 2003-07-29

ApplicantMedimop Medical Projects, Ltd.
Decision Date2003-07-29
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIX2VIAL TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2003-07-29 under 510(k) number K031861. 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 MIX2VIAL TRANSFER DEVICE?

MIX2VIAL TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 2003-07-29. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K031861.

When did MIX2VIAL TRANSFER DEVICE receive FDA 510(k) clearance?

MIX2VIAL TRANSFER DEVICE received FDA 510(k) clearance on 2003-07-29, under 510(k) number K031861.

Who is the listed applicant for MIX2VIAL TRANSFER DEVICE?

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

What is the FDA product code for MIX2VIAL TRANSFER DEVICE?

The FDA product code for MIX2VIAL TRANSFER DEVICE is LHI.

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Other records listing Medimop Medical Projects, Ltd. as applicant

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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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