ACUTE PERITONEAL DIALYSIS KIT— 510(k) K870472

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K870472 for ACUTE PERITONEAL DIALYSIS KIT, Substantially Equivalent on 1987-02-25. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code FKO
Advisory panel: Gastroenterology, Urology
Date received: 1987-02-03
Decision date: 1987-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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Adverse events under product code FKO

product code FKO

Other: 1
Total: 1

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.