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FDA 510(k)

TUBE FEEDING CONTAINER 1500 ML DISPOSE.

K-Number: K800955 · 1980-05-30

Decision Date1980-05-30
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBE FEEDING CONTAINER 1500 ML DISPOSE. is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1980-05-30 under 510(k) number K800955. 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 TUBE FEEDING CONTAINER 1500 ML DISPOSE.?

TUBE FEEDING CONTAINER 1500 ML DISPOSE. is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K800955.

When did TUBE FEEDING CONTAINER 1500 ML DISPOSE. receive FDA 510(k) clearance?

TUBE FEEDING CONTAINER 1500 ML DISPOSE. received FDA 510(k) clearance on 1980-05-30, under 510(k) number K800955.

Who is the listed applicant for TUBE FEEDING CONTAINER 1500 ML DISPOSE.?

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

What is the FDA product code for TUBE FEEDING CONTAINER 1500 ML DISPOSE.?

The FDA product code for TUBE FEEDING CONTAINER 1500 ML DISPOSE. 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 The Healthcare Group Laboratories, 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.

View all 29 devices →

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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