MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES— 510(k) K990379

Substantially Equivalent

Dexide, Inc.

FDA 510(k) clearance K990379 for MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES, Substantially Equivalent on 1999-03-04. Applicant: Dexide, Inc..

Clearance details

Applicant: Dexide, Inc.
Product code: Code GCJ
Advisory panel: Gastroenterology, Urology
Date received: 1999-02-08
Decision date: 1999-03-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GCJ

product code GCJ

Death: 39
Injury: 1,638
Malfunction: 28,216
Other: 11
Total: 29,904

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.