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FDA 510(k)

VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM

K-Number: K073241 · 2008-02-08

ApplicantVascular Pathways
Decision Date2008-02-08
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Pathways. It received FDA 510(k) clearance on 2008-02-08 under 510(k) number K073241. 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 VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM?

VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM is a medical device that received FDA 510(k) clearance on 2008-02-08. The listed applicant is Vascular Pathways. The 510(k) number is K073241.

When did VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM receive FDA 510(k) clearance?

VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM received FDA 510(k) clearance on 2008-02-08, under 510(k) number K073241.

Who is the listed applicant for VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM?

The FDA 510(k) record lists Vascular Pathways as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM?

The FDA product code for VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM is FOZ.

Related Clinical Trials

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.

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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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