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FDA 510(k)

MIC TRANSGASTRIC JEJUNAL TUBE

K-Number: K926581 · 1994-09-28

Decision Date1994-09-28
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MIC TRANSGASTRIC JEJUNAL TUBE 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 1994-09-28 under 510(k) number K926581. 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 MIC TRANSGASTRIC JEJUNAL TUBE?

MIC TRANSGASTRIC JEJUNAL TUBE is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is Medical Innovations Corp.. The 510(k) number is K926581.

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

MIC TRANSGASTRIC JEJUNAL TUBE received FDA 510(k) clearance on 1994-09-28, under 510(k) number K926581.

Who is the listed applicant for MIC TRANSGASTRIC JEJUNAL TUBE?

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 TUBE?

The FDA product code for MIC TRANSGASTRIC JEJUNAL 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 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.

View all 24 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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