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FDA 510(k)

MAXIFILL TRANSFER SET

K-Number: K842345 · 1984-08-17

ApplicantLyphomed, Inc.
Decision Date1984-08-17
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAXIFILL TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Lyphomed, Inc.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842345. 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 MAXIFILL TRANSFER SET?

MAXIFILL TRANSFER SET is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Lyphomed, Inc.. The 510(k) number is K842345.

When did MAXIFILL TRANSFER SET receive FDA 510(k) clearance?

MAXIFILL TRANSFER SET received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842345.

Who is the listed applicant for MAXIFILL TRANSFER SET?

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

What is the FDA product code for MAXIFILL TRANSFER SET?

The FDA product code for MAXIFILL TRANSFER SET is LHI.

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Other records listing Lyphomed, Inc. 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.

K910142SPARK KIT(R), MODIFICATIONK864509SPARK-KIT(TM)K853019NITROGLYCERIN INFUSION SETK853086SECONDARY ADMINISTRATION SETK852882MAXIFILL TRANSFER SETK852881VENTED SECONDARY IV ADMINISTRATION SET

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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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