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FDA 510(k)

VIGGO NEOFLON INFUSION CANNULA

K-Number: K850276 · 1985-04-12

ApplicantViggo Products
Decision Date1985-04-12
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIGGO NEOFLON INFUSION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Viggo Products. It received FDA 510(k) clearance on 1985-04-12 under 510(k) number K850276. 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 VIGGO NEOFLON INFUSION CANNULA?

VIGGO NEOFLON INFUSION CANNULA is a medical device that received FDA 510(k) clearance on 1985-04-12. The listed applicant is Viggo Products. The 510(k) number is K850276.

When did VIGGO NEOFLON INFUSION CANNULA receive FDA 510(k) clearance?

VIGGO NEOFLON INFUSION CANNULA received FDA 510(k) clearance on 1985-04-12, under 510(k) number K850276.

Who is the listed applicant for VIGGO NEOFLON INFUSION CANNULA?

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

What is the FDA product code for VIGGO NEOFLON INFUSION CANNULA?

The FDA product code for VIGGO NEOFLON INFUSION CANNULA is FOZ.

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Other records listing Viggo Products 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.

K850769VIGGO ACCESSORIES FOR I.V. THERAPYK850277VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.K850280VIGGO CONNECTA 3-WAY INFUSION STOPCOCKK850460VIGGO SECALON T CATHETERK850278VASCULON I.V. CANNULAEK850349VIGGO ARTERIAL CANNULA

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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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