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FDA 510(k)

NUTRI-CATH - FEEDING TUBE

K-Number: K861090 · 1986-06-18

Decision Date1986-06-18
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NUTRI-CATH - FEEDING TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Gesco Intl., Inc.. It received FDA 510(k) clearance on 1986-06-18 under 510(k) number K861090. 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 NUTRI-CATH - FEEDING TUBE?

NUTRI-CATH - FEEDING TUBE is a medical device that received FDA 510(k) clearance on 1986-06-18. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K861090.

When did NUTRI-CATH - FEEDING TUBE receive FDA 510(k) clearance?

NUTRI-CATH - FEEDING TUBE received FDA 510(k) clearance on 1986-06-18, under 510(k) number K861090.

Who is the listed applicant for NUTRI-CATH - FEEDING TUBE?

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

What is the FDA product code for NUTRI-CATH - FEEDING TUBE?

The FDA product code for NUTRI-CATH - FEEDING TUBE 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 Gesco Intl., 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 26 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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