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FDA 510(k)

ONAT BALLOONED NASOGASTRIC TUBE

K-Number: K920262 · 1993-04-20

Decision Date1993-04-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ONAT BALLOONED NASOGASTRIC TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Macdonald Medical Devices, Inc.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K920262. 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 ONAT BALLOONED NASOGASTRIC TUBE?

ONAT BALLOONED NASOGASTRIC TUBE is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Macdonald Medical Devices, Inc.. The 510(k) number is K920262.

When did ONAT BALLOONED NASOGASTRIC TUBE receive FDA 510(k) clearance?

ONAT BALLOONED NASOGASTRIC TUBE received FDA 510(k) clearance on 1993-04-20, under 510(k) number K920262.

Who is the listed applicant for ONAT BALLOONED NASOGASTRIC TUBE?

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

What is the FDA product code for ONAT BALLOONED NASOGASTRIC TUBE?

The FDA product code for ONAT BALLOONED NASOGASTRIC 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.

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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