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FDA 510(k)

VASCULON II I.V. CATHETER

K-Number: K811171 · 1981-05-27

ApplicantPioneer Viggo, Inc.
Decision Date1981-05-27
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VASCULON II I.V. CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Viggo, Inc.. It received FDA 510(k) clearance on 1981-05-27 under 510(k) number K811171. 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 VASCULON II I.V. CATHETER?

VASCULON II I.V. CATHETER is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Pioneer Viggo, Inc.. The 510(k) number is K811171.

When did VASCULON II I.V. CATHETER receive FDA 510(k) clearance?

VASCULON II I.V. CATHETER received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811171.

Who is the listed applicant for VASCULON II I.V. CATHETER?

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

What is the FDA product code for VASCULON II I.V. CATHETER?

The FDA product code for VASCULON II I.V. CATHETER 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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Other records listing Pioneer Viggo, 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.

K823120EXACTA & CONNECTA STOPCOCKS W/EXTENSIONK813454I.V. FILTER-PREVENTK812159INTRAVASCULAR CATHETERK801537START IT WITH & WITHOUT I.V. CATH. UNITK791809BLOOD TRANSFUSION MICROFILTER

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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