CURITY SILICONE NEPHROSTOMY CATHETER— 510(k) K842840

Substantially Equivalent

The Kendal Co.

FDA 510(k) clearance K842840 for CURITY SILICONE NEPHROSTOMY CATHETER, Substantially Equivalent on 1984-10-04. Applicant: The Kendal Co..

Clearance details

Applicant: The Kendal Co.
Product code: Code LJE
Advisory panel: Unknown
Date received: 1984-07-20
Decision date: 1984-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code LJE

product code LJE

Death: 6
Total: 6

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.