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FDA 510(k)

LEONARD/NORTON HYPERALIMENTATION CATHET.

K-Number: K821679 · 1982-07-02

ApplicantNorton Performance Plastics Corp.
Decision Date1982-07-02
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEONARD/NORTON HYPERALIMENTATION CATHET. 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 1982-07-02 under 510(k) number K821679. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEONARD/NORTON HYPERALIMENTATION CATHET.?

LEONARD/NORTON HYPERALIMENTATION CATHET. is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K821679.

When did LEONARD/NORTON HYPERALIMENTATION CATHET. receive FDA 510(k) clearance?

LEONARD/NORTON HYPERALIMENTATION CATHET. received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821679.

Who is the listed applicant for LEONARD/NORTON HYPERALIMENTATION CATHET.?

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 LEONARD/NORTON HYPERALIMENTATION CATHET.?

The FDA product code for LEONARD/NORTON HYPERALIMENTATION CATHET. is FOZ.

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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 FLOK842858FLUID ADMINISTRATION LINE W/SPIKE 14-923K841828CENTRAL VENOUS CATHETER W/BIG-GARDK840240MICROFUSE INTRAVENOUS CATHETER SET

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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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