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FDA 510(k)

TRI-MED QUICK-STEP GASTRIC LAVAGE KIT

K-Number: K920527 · 1992-09-04

Decision Date1992-09-04
Product CodeKDH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRI-MED QUICK-STEP GASTRIC LAVAGE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med Specialties, Inc.. It received FDA 510(k) clearance on 1992-09-04 under 510(k) number K920527. The device is classified under product code KDH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI-MED QUICK-STEP GASTRIC LAVAGE KIT?

TRI-MED QUICK-STEP GASTRIC LAVAGE KIT is a medical device that received FDA 510(k) clearance on 1992-09-04. The listed applicant is Tri-Med Specialties, Inc.. The 510(k) number is K920527.

When did TRI-MED QUICK-STEP GASTRIC LAVAGE KIT receive FDA 510(k) clearance?

TRI-MED QUICK-STEP GASTRIC LAVAGE KIT received FDA 510(k) clearance on 1992-09-04, under 510(k) number K920527.

Who is the listed applicant for TRI-MED QUICK-STEP GASTRIC LAVAGE KIT?

The FDA 510(k) record lists Tri-Med Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRI-MED QUICK-STEP GASTRIC LAVAGE KIT?

The FDA product code for TRI-MED QUICK-STEP GASTRIC LAVAGE KIT is KDH.

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 Tri-Med Specialties, Inc. 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.

View all 14 devices →

Related Devices (Code: KDH)

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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