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FDA 510(k)

RECTAL LEAKAGE INHIBITOR

K-Number: K792597 · 1980-02-06

ApplicantAugustin Jones, M.D.
Decision Date1980-02-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RECTAL LEAKAGE INHIBITOR is the device name listed in this FDA 510(k) record. The listed applicant is Augustin Jones, M.D.. It received FDA 510(k) clearance on 1980-02-06 under 510(k) number K792597. 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 RECTAL LEAKAGE INHIBITOR?

RECTAL LEAKAGE INHIBITOR is a medical device that received FDA 510(k) clearance on 1980-02-06. The listed applicant is Augustin Jones, M.D.. The 510(k) number is K792597.

When did RECTAL LEAKAGE INHIBITOR receive FDA 510(k) clearance?

RECTAL LEAKAGE INHIBITOR received FDA 510(k) clearance on 1980-02-06, under 510(k) number K792597.

Who is the listed applicant for RECTAL LEAKAGE INHIBITOR?

The FDA 510(k) record lists Augustin Jones, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RECTAL LEAKAGE INHIBITOR?

The FDA product code for RECTAL LEAKAGE INHIBITOR is KNT.

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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.

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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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