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FDA 510(k)

MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY

K-Number: K100366 · 2010-06-14

Decision Date2010-06-14
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY is the device name listed in this FDA 510(k) record. The listed applicant is Maxter Catheters. It received FDA 510(k) clearance on 2010-06-14 under 510(k) number K100366. 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 MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY?

MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY is a medical device that received FDA 510(k) clearance on 2010-06-14. The listed applicant is Maxter Catheters. The 510(k) number is K100366.

When did MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY receive FDA 510(k) clearance?

MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY received FDA 510(k) clearance on 2010-06-14, under 510(k) number K100366.

Who is the listed applicant for MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY?

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

What is the FDA product code for MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY?

The FDA product code for MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY 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.

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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