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FDA 510(k)

FLUID ADMINISTRATION LINE W/SPIKE 14-923

K-Number: K842858 · 1984-09-11

ApplicantNorton Performance Plastics Corp.
Decision Date1984-09-11
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLUID ADMINISTRATION LINE W/SPIKE 14-923 is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1984-09-11 under 510(k) number K842858. 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 FLUID ADMINISTRATION LINE W/SPIKE 14-923?

FLUID ADMINISTRATION LINE W/SPIKE 14-923 is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K842858.

When did FLUID ADMINISTRATION LINE W/SPIKE 14-923 receive FDA 510(k) clearance?

FLUID ADMINISTRATION LINE W/SPIKE 14-923 received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842858.

Who is the listed applicant for FLUID ADMINISTRATION LINE W/SPIKE 14-923?

The FDA 510(k) record lists Norton Performance Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUID ADMINISTRATION LINE W/SPIKE 14-923?

The FDA product code for FLUID ADMINISTRATION LINE W/SPIKE 14-923 is FPA.

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Other records listing Norton Performance Plastics Corp. 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.

K853791NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000K852914ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSIONK851299CORRECT FLOK841828CENTRAL VENOUS CATHETER W/BIG-GARDK840240MICROFUSE INTRAVENOUS CATHETER SETK831587TEMP. REPAIR KIT-DUAL LUMEN CATHETER

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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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