CITRISOL ACID CONCENTRATE— 510(k) K130511

Substantially Equivalent

Diasol, Inc.

FDA 510(k) clearance K130511 for CITRISOL ACID CONCENTRATE, Substantially Equivalent on 2014-02-10. Applicant: Diasol, Inc..

Clearance details

Applicant: Diasol, Inc.
Product code: Code KPO
Advisory panel: Gastroenterology, Urology
Date received: 2013-02-27
Decision date: 2014-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Fernando, CA, US

Download summary PDF View on FDA.gov ↗

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.