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FDA 510(k)

ANTHRON CATHETERS & SETS

K-Number: K861117 · 1986-06-18

ApplicantToray Industries (America), Inc.
Decision Date1986-06-18
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANTHRON CATHETERS & SETS is the device name listed in this FDA 510(k) record. The listed applicant is Toray Industries (America), Inc.. It received FDA 510(k) clearance on 1986-06-18 under 510(k) number K861117. 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 CATHETERS & SETS?

ANTHRON CATHETERS & SETS is a medical device that received FDA 510(k) clearance on 1986-06-18. The listed applicant is Toray Industries (America), Inc.. The 510(k) number is K861117.

When did ANTHRON CATHETERS & SETS receive FDA 510(k) clearance?

ANTHRON CATHETERS & SETS received FDA 510(k) clearance on 1986-06-18, under 510(k) number K861117.

Who is the listed applicant for ANTHRON CATHETERS & SETS?

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

What is the FDA product code for ANTHRON CATHETERS & SETS?

The FDA product code for ANTHRON CATHETERS & SETS is FOZ.

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Other records listing Toray Industries (America), 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.

K042370TORAYGUIDE GUIDEWIREK030050TORAYSULFONE DIALYZER, BS-L SERIESK002512TORAYSULFONE DIALYZERK994198HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0LK942681FILTRYZERK935471FILTRYZER(TM)

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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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