URETERAL DILATOR— 510(k) K852324

Substantially Equivalent

American Edwards Laboratories

FDA 510(k) clearance K852324 for URETERAL DILATOR, Substantially Equivalent on 1985-08-21. Applicant: American Edwards Laboratories.

Clearance details

Applicant: American Edwards Laboratories
Product code: Code EZN
Advisory panel: Gastroenterology, Urology
Date received: 1985-05-30
Decision date: 1985-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EZN

product code EZN

Death: 3
Injury: 127
Total: 130

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.