FDA 510(k)

VYGON NUTRILINE CATHETERS

K-Number: K051690 · 2005-08-19

Decision Date2005-08-19

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VYGON NUTRILINE CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 2005-08-19 under 510(k) number K051690. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON NUTRILINE CATHETERS?

VYGON NUTRILINE CATHETERS is a medical device that received FDA 510(k) clearance on 2005-08-19. The listed applicant is Vygon Corp.. The 510(k) number is K051690.

When did VYGON NUTRILINE CATHETERS receive FDA 510(k) clearance?

VYGON NUTRILINE CATHETERS received FDA 510(k) clearance on 2005-08-19, under 510(k) number K051690.

Who is the listed applicant for VYGON NUTRILINE CATHETERS?

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 NUTRILINE CATHETERS?

The FDA product code for VYGON NUTRILINE CATHETERS is LJS.

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Other records listing Vygon Corp. as applicant

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Related Devices (Code: LJS)

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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.