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FDA 510(k)

GASTRIC LAVAGE VALVE

K-Number: K990365 · 2000-07-26

ApplicantT-Med Vac Corporation
Decision Date2000-07-26
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTRIC LAVAGE VALVE is the device name listed in this FDA 510(k) record. The listed applicant is T-Med Vac Corporation. It received FDA 510(k) clearance on 2000-07-26 under 510(k) number K990365. 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 GASTRIC LAVAGE VALVE?

GASTRIC LAVAGE VALVE is a medical device that received FDA 510(k) clearance on 2000-07-26. The listed applicant is T-Med Vac Corporation. The 510(k) number is K990365.

When did GASTRIC LAVAGE VALVE receive FDA 510(k) clearance?

GASTRIC LAVAGE VALVE received FDA 510(k) clearance on 2000-07-26, under 510(k) number K990365.

Who is the listed applicant for GASTRIC LAVAGE VALVE?

The FDA 510(k) record lists T-Med Vac Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GASTRIC LAVAGE VALVE?

The FDA product code for GASTRIC LAVAGE VALVE 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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