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FDA 510(k)

VIAL2BAG

K-Number: K072759 · 2007-12-13

ApplicantMedimop Medical Projects, Ltd.
Decision Date2007-12-13
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIAL2BAG 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 2007-12-13 under 510(k) number K072759. 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 VIAL2BAG?

VIAL2BAG is a medical device that received FDA 510(k) clearance on 2007-12-13. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K072759.

When did VIAL2BAG receive FDA 510(k) clearance?

VIAL2BAG received FDA 510(k) clearance on 2007-12-13, under 510(k) number K072759.

Who is the listed applicant for VIAL2BAG?

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 VIAL2BAG?

The FDA product code for VIAL2BAG is LHI.

Other records listing Medimop Medical Projects, 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.

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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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