DISPOSABLE PERITONEAL DIALYSIS EXTENSION— 510(k) K791722

Substantially Equivalent

American Medical Products, Inc.

FDA 510(k) clearance K791722 for DISPOSABLE PERITONEAL DIALYSIS EXTENSION, Substantially Equivalent on 1979-11-16. Applicant: American Medical Products, Inc..

Clearance details

Applicant: American Medical Products, Inc.
Product code: Code KDJ
Advisory panel: Gastroenterology, Urology
Date received: 1979-08-30
Decision date: 1979-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KDJ

product code KDJ

Death: 298
Injury: 9,221
Malfunction: 8,438
Other: 1
Total: 17,958

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.