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FDA 510(k)

VYGON LATEX FREE BIONECTOR

K-Number: K052881 · 2006-03-02

ApplicantVygon Corp.
Decision Date2006-03-02
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VYGON LATEX FREE BIONECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 2006-03-02 under 510(k) number K052881. 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 VYGON LATEX FREE BIONECTOR?

VYGON LATEX FREE BIONECTOR is a medical device that received FDA 510(k) clearance on 2006-03-02. The listed applicant is Vygon Corp.. The 510(k) number is K052881.

When did VYGON LATEX FREE BIONECTOR receive FDA 510(k) clearance?

VYGON LATEX FREE BIONECTOR received FDA 510(k) clearance on 2006-03-02, under 510(k) number K052881.

Who is the listed applicant for VYGON LATEX FREE BIONECTOR?

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

What is the FDA product code for VYGON LATEX FREE BIONECTOR?

The FDA product code for VYGON LATEX FREE BIONECTOR is FOZ.

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Other records listing Vygon Corp. 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.

K121105NUTRISAFE 2 FEEDING TUBEK100163NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXXK073493HEPATOSTAT SETK070705MODIFICATION TO: LATEX-FREE BIONECTOR, MODEL# 896.019, 896.039K061796HEPATOSTAT SET, MODEL 760XK061250MULTICATH EXPERT

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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.

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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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