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FDA 510(k)

MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT

K-Number: K921652 · 1994-05-02

Decision Date1994-05-02
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Innovations Corp.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K921652. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT?

MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Medical Innovations Corp.. The 510(k) number is K921652.

When did MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT receive FDA 510(k) clearance?

MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT received FDA 510(k) clearance on 1994-05-02, under 510(k) number K921652.

Who is the listed applicant for MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT?

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

What is the FDA product code for MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT?

The FDA product code for MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT 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 Medical Innovations Corp. 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.

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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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