CROSSPOINT TRANSACCESS CATHETER— 510(k) K013363

Substantially Equivalent

Trans Vascular Incorporated

FDA 510(k) clearance K013363 for CROSSPOINT TRANSACCESS CATHETER, Substantially Equivalent on 2002-04-02. Applicant: Trans Vascular Incorporated.

Clearance details

Applicant: Trans Vascular Incorporated
Product code: Code ITX
Advisory panel: Radiology
Date received: 2001-10-10
Decision date: 2002-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.