GESCO DUAL LUMEN UMBILICATH II-DL— 510(k) K896041

Unknown

Gesco Intl., Inc.

FDA 510(k) clearance K896041 for GESCO DUAL LUMEN UMBILICATH II-DL, Unknown on 1990-04-17. Applicant: Gesco Intl., Inc..

Clearance details

Applicant: Gesco Intl., Inc.
Product code: Code FOS
Advisory panel: General Hospital
Date received: 1989-10-17
Decision date: 1990-04-17
Decision: Unknown
Clearance type: Traditional
Location: San Antonio, TX, US

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Adverse events under product code FOS

product code FOS

Death: 12
Other: 1
Total: 13

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.