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FDA 510(k)

MICROFUSE INTRAVENOUS CATHETER SET

K-Number: K840240 · 1984-04-17

ApplicantNorton Performance Plastics Corp.
Decision Date1984-04-17
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROFUSE INTRAVENOUS CATHETER SET 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 1984-04-17 under 510(k) number K840240. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROFUSE INTRAVENOUS CATHETER SET?

MICROFUSE INTRAVENOUS CATHETER SET is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K840240.

When did MICROFUSE INTRAVENOUS CATHETER SET receive FDA 510(k) clearance?

MICROFUSE INTRAVENOUS CATHETER SET received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840240.

Who is the listed applicant for MICROFUSE INTRAVENOUS CATHETER SET?

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 MICROFUSE INTRAVENOUS CATHETER SET?

The FDA product code for MICROFUSE INTRAVENOUS CATHETER SET is DQY.

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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-GARDK831587TEMP. REPAIR KIT-DUAL LUMEN CATHETER

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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