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FDA 510(k)

NASOGRASTRIC TUBBE HOLDER

K-Number: K922209 · 1992-10-30

Decision Date1992-10-30
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NASOGRASTRIC TUBBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Design Corp.. It received FDA 510(k) clearance on 1992-10-30 under 510(k) number K922209. 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 NASOGRASTRIC TUBBE HOLDER?

NASOGRASTRIC TUBBE HOLDER is a medical device that received FDA 510(k) clearance on 1992-10-30. The listed applicant is Innovative Medical Design Corp.. The 510(k) number is K922209.

When did NASOGRASTRIC TUBBE HOLDER receive FDA 510(k) clearance?

NASOGRASTRIC TUBBE HOLDER received FDA 510(k) clearance on 1992-10-30, under 510(k) number K922209.

Who is the listed applicant for NASOGRASTRIC TUBBE HOLDER?

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

What is the FDA product code for NASOGRASTRIC TUBBE HOLDER?

The FDA product code for NASOGRASTRIC TUBBE HOLDER 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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