C-PORT— 510(k) K030636

Substantially Equivalent

Clinisurg Vascular Products, LLC

FDA 510(k) clearance K030636 for C-PORT, Substantially Equivalent on 2003-06-05. Applicant: Clinisurg Vascular Products, LLC.

Clearance details

Applicant: Clinisurg Vascular Products, LLC
Product code: Code LJT
Advisory panel: General Hospital
Date received: 2003-02-28
Decision date: 2003-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LJT

product code LJT

Death: 234
Injury: 6,468
Malfunction: 5,326
Other: 2
Total: 12,030

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.