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FDA 510(k)

VYGON ENTERNAL NUTRITION TUBES

K-Number: K820176 · 1982-02-05

ApplicantExco, Inc.
Decision Date1982-02-05
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VYGON ENTERNAL NUTRITION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820176. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON ENTERNAL NUTRITION TUBES?

VYGON ENTERNAL NUTRITION TUBES is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Exco, Inc.. The 510(k) number is K820176.

When did VYGON ENTERNAL NUTRITION TUBES receive FDA 510(k) clearance?

VYGON ENTERNAL NUTRITION TUBES received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820176.

Who is the listed applicant for VYGON ENTERNAL NUTRITION TUBES?

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

What is the FDA product code for VYGON ENTERNAL NUTRITION TUBES?

The FDA product code for VYGON ENTERNAL NUTRITION TUBES is KNT.

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.

Other records listing Exco, 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.

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Related Devices (Code: KNT)

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.

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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