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FDA 510(k)

I.V. TRANSFER SPIKE

K-Number: K842678 · 1984-10-09

ApplicantLyphomed, Inc.
Decision Date1984-10-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. TRANSFER SPIKE is the device name listed in this FDA 510(k) record. The listed applicant is Lyphomed, Inc.. It received FDA 510(k) clearance on 1984-10-09 under 510(k) number K842678. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. TRANSFER SPIKE?

I.V. TRANSFER SPIKE is a medical device that received FDA 510(k) clearance on 1984-10-09. The listed applicant is Lyphomed, Inc.. The 510(k) number is K842678.

When did I.V. TRANSFER SPIKE receive FDA 510(k) clearance?

I.V. TRANSFER SPIKE received FDA 510(k) clearance on 1984-10-09, under 510(k) number K842678.

Who is the listed applicant for I.V. TRANSFER SPIKE?

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 I.V. TRANSFER SPIKE?

The FDA product code for I.V. TRANSFER SPIKE is FPA.

Related Clinical Trials

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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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: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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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