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FDA 510(k)

ENTERAL FEEDING CONTAINER

K-Number: K852966 · 1985-08-27

Decision Date1985-08-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Empire Industries, Inc.. It received FDA 510(k) clearance on 1985-08-27 under 510(k) number K852966. 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 ENTERAL FEEDING CONTAINER?

ENTERAL FEEDING CONTAINER is a medical device that received FDA 510(k) clearance on 1985-08-27. The listed applicant is Empire Industries, Inc.. The 510(k) number is K852966.

When did ENTERAL FEEDING CONTAINER receive FDA 510(k) clearance?

ENTERAL FEEDING CONTAINER received FDA 510(k) clearance on 1985-08-27, under 510(k) number K852966.

Who is the listed applicant for ENTERAL FEEDING CONTAINER?

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

What is the FDA product code for ENTERAL FEEDING CONTAINER?

The FDA product code for ENTERAL FEEDING CONTAINER 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 Empire Industries, 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.

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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