SOLEX CATHETER, MODEL SL2593— 510(k) K081936

Substantially Equivalent

Alsius Corp.

FDA 510(k) clearance K081936 for SOLEX CATHETER, MODEL SL2593, Substantially Equivalent on 2008-08-13. Applicant: Alsius Corp..

Clearance details

Applicant: Alsius Corp.
Product code: Code NCX
Advisory panel: Cardiovascular
Date received: 2008-07-07
Decision date: 2008-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NCX

product code NCX

Death: 30
Malfunction: 2,302
Total: 2,332

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.