Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE

K-Number: K862489 · 1986-09-23

Decision Date1986-09-23
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE is the device name listed in this FDA 510(k) record. The listed applicant is Knight Medical, Inc.. It received FDA 510(k) clearance on 1986-09-23 under 510(k) number K862489. 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 SETS FOR GRAVITY AND PUMP USE?

ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE is a medical device that received FDA 510(k) clearance on 1986-09-23. The listed applicant is Knight Medical, Inc.. The 510(k) number is K862489.

When did ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE receive FDA 510(k) clearance?

ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE received FDA 510(k) clearance on 1986-09-23, under 510(k) number K862489.

Who is the listed applicant for ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE?

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

What is the FDA product code for ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE?

The FDA product code for ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE 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 Knight Medical, 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑