ESOPHAGEAL OVERTUBE— 510(k) K890629

Name: FDA 510(k) clearance K890629
Creator: U.S. Food and Drug Administration
Published: 1989-05-31

Substantially Equivalent

Gastrotech, Inc.

FDA 510(k) clearance K890629 for ESOPHAGEAL OVERTUBE, Substantially Equivalent on 1989-05-31. Applicant: Gastrotech, Inc.. Device class: 2.

Clearance details

Applicant: Gastrotech, Inc.
Product code: Code FED
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1989-02-10
Decision date: 1989-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Independence, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FED

product code FED

Death: 10
Total: 10

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.