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FDA 510(k)

LOW VOLUME BIFURCATED IV EXTENSION SET

K-Number: K901088 · 1990-10-04

ApplicantMarquette Medical, Inc.
Decision Date1990-10-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOW VOLUME BIFURCATED IV EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical, Inc.. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K901088. 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 LOW VOLUME BIFURCATED IV EXTENSION SET?

LOW VOLUME BIFURCATED IV EXTENSION SET is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Marquette Medical, Inc.. The 510(k) number is K901088.

When did LOW VOLUME BIFURCATED IV EXTENSION SET receive FDA 510(k) clearance?

LOW VOLUME BIFURCATED IV EXTENSION SET received FDA 510(k) clearance on 1990-10-04, under 510(k) number K901088.

Who is the listed applicant for LOW VOLUME BIFURCATED IV EXTENSION SET?

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

What is the FDA product code for LOW VOLUME BIFURCATED IV EXTENSION SET?

The FDA product code for LOW VOLUME BIFURCATED IV EXTENSION SET is FPA.

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Other records listing Marquette Medical, 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.

K021471MARQUETTE HUBER TRAP SAFETY INFUSION SETK953008INFANT FEEDING TUBEK952976PLASTIC BLUNT CANNULAK920537SUBCUTANEOUS INFUSION SETK9052194' LOW VOLUME IV EXTENSION SETK9052184 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP

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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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