MEDIFIX URETEROSCOPE— 510(k) K011325

Substantially Equivalent

Medifix, Inc.

FDA 510(k) clearance K011325 for MEDIFIX URETEROSCOPE, Substantially Equivalent on 2001-07-25. Applicant: Medifix, Inc..

Clearance details

Applicant: Medifix, Inc.
Product code: Code FGB
Advisory panel: Gastroenterology, Urology
Date received: 2001-05-01
Decision date: 2001-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morton Grove, IL, US

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Adverse events under product code FGB

product code FGB

Death: 6
Injury: 552
Malfunction: 3,922
Other: 1
Total: 4,481

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.