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FDA 510(k)

VIGGO SECALON T CATHETER

K-Number: K850460 · 1985-04-11

ApplicantViggo Products
Decision Date1985-04-11
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIGGO SECALON T CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Viggo Products. It received FDA 510(k) clearance on 1985-04-11 under 510(k) number K850460. 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 SECALON T CATHETER?

VIGGO SECALON T CATHETER is a medical device that received FDA 510(k) clearance on 1985-04-11. The listed applicant is Viggo Products. The 510(k) number is K850460.

When did VIGGO SECALON T CATHETER receive FDA 510(k) clearance?

VIGGO SECALON T CATHETER received FDA 510(k) clearance on 1985-04-11, under 510(k) number K850460.

Who is the listed applicant for VIGGO SECALON T CATHETER?

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 SECALON T CATHETER?

The FDA product code for VIGGO SECALON T CATHETER 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. THERAPYK850276VIGGO NEOFLON INFUSION CANNULAK850277VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.K850280VIGGO CONNECTA 3-WAY INFUSION STOPCOCKK850278VASCULON 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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