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FDA 510(k)

EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS

K-Number: K842133 · 1985-02-19

ApplicantCardio Search, Inc.
Decision Date1985-02-19
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Search, Inc.. It received FDA 510(k) clearance on 1985-02-19 under 510(k) number K842133. 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 EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS?

EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS is a medical device that received FDA 510(k) clearance on 1985-02-19. The listed applicant is Cardio Search, Inc.. The 510(k) number is K842133.

When did EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS receive FDA 510(k) clearance?

EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS received FDA 510(k) clearance on 1985-02-19, under 510(k) number K842133.

Who is the listed applicant for EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS?

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

What is the FDA product code for EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS?

The FDA product code for EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS is FOZ.

Related Clinical Trials

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Other records listing Cardio Search, 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.

K841880ERYTHROCATH UMBILICAL CATHETERK833873CARDIOSEARCH RIGHT ATRIAL CATH-K832064VENOUS CATHETER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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