CANNON II PLUS— 510(k) K040078

Unknown

Arrow International, Inc.

FDA 510(k) clearance K040078 for CANNON II PLUS, Unknown on 2004-02-13. Applicant: Arrow International, Inc..

Clearance details

Applicant: Arrow International, Inc.
Product code: Code MSD
Advisory panel: Gastroenterology, Urology
Date received: 2004-01-14
Decision date: 2004-02-13
Decision: Unknown
Clearance type: Special
Location: Reading, PA, US

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Adverse events under product code MSD

product code MSD

Death: 67
Injury: 545
Malfunction: 3,661
Total: 4,273

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.