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FDA 510(k)

ANTHRON CATHETER SET

K-Number: K802918 · 1981-04-21

ApplicantNational Catheter Co. Div. Mallinckrodt
Decision Date1981-04-21
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANTHRON CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is National Catheter Co. Div. Mallinckrodt. It received FDA 510(k) clearance on 1981-04-21 under 510(k) number K802918. 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 ANTHRON CATHETER SET?

ANTHRON CATHETER SET is a medical device that received FDA 510(k) clearance on 1981-04-21. The listed applicant is National Catheter Co. Div. Mallinckrodt. The 510(k) number is K802918.

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

ANTHRON CATHETER SET received FDA 510(k) clearance on 1981-04-21, under 510(k) number K802918.

Who is the listed applicant for ANTHRON CATHETER SET?

The FDA 510(k) record lists National Catheter Co. Div. Mallinckrodt as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTHRON CATHETER SET?

The FDA product code for ANTHRON CATHETER SET is FOZ.

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Other records listing National Catheter Co. Div. Mallinckrodt 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.

K802505DOUBLE LUMEN TRACHEAL TUBEK810321REINFORCED TRACHEOSTOMY TUBE SET(TENTAT)K801924HI-LO TEMP GEN. PURPOSE TEMP. PROBEK801005MLT TUBE MICROLARYNGEAL TRACHEAL TUBE)K791190STETHOSCOPE WITH TEMPERATURE SENSORK781665TUBE, LEATHERMAN/IMBRUCE

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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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