HEMODIALYSIS BATH CONCENTRATE SOLUTIONS FOR HEMODI— 510(k) K864265

Substantially Equivalent

Dial Medical of Florida, Inc.

FDA 510(k) clearance K864265 for HEMODIALYSIS BATH CONCENTRATE SOLUTIONS FOR HEMODI, Substantially Equivalent on 1987-03-17. Applicant: Dial Medical of Florida, Inc..

Clearance details

Applicant: Dial Medical of Florida, Inc.
Product code: Code KPO
Advisory panel: Gastroenterology, Urology
Date received: 1986-10-29
Decision date: 1987-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deland, FL, US

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Adverse events under product code KPO

product code KPO

Death: 14
Malfunction: 775
Other: 20
Total: 809

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.