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FDA 510(k)

INTRO-REDUCER (NASOGASTRIC TUBE)

K-Number: K875232 · 1988-06-02

Decision Date1988-06-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INTRO-REDUCER (NASOGASTRIC TUBE) is the device name listed in this FDA 510(k) record. The listed applicant is Health Improvement Assoc.. It received FDA 510(k) clearance on 1988-06-02 under 510(k) number K875232. 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 INTRO-REDUCER (NASOGASTRIC TUBE)?

INTRO-REDUCER (NASOGASTRIC TUBE) is a medical device that received FDA 510(k) clearance on 1988-06-02. The listed applicant is Health Improvement Assoc.. The 510(k) number is K875232.

When did INTRO-REDUCER (NASOGASTRIC TUBE) receive FDA 510(k) clearance?

INTRO-REDUCER (NASOGASTRIC TUBE) received FDA 510(k) clearance on 1988-06-02, under 510(k) number K875232.

Who is the listed applicant for INTRO-REDUCER (NASOGASTRIC TUBE)?

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

What is the FDA product code for INTRO-REDUCER (NASOGASTRIC TUBE)?

The FDA product code for INTRO-REDUCER (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.

Other records listing Health Improvement Assoc. 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.

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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