MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER— 510(k) K103110

Substantially Equivalent

Abbott Vascular-Cardiac Therapies

FDA 510(k) clearance K103110 for MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER, Substantially Equivalent on 2011-01-10. Applicant: Abbott Vascular-Cardiac Therapies.

Clearance details

Applicant: Abbott Vascular-Cardiac Therapies
Product code: Code LOX
Advisory panel: Cardiovascular
Date received: 2010-10-08
Decision date: 2011-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LOX

product code LOX

Death: 190
Injury: 1,498
Malfunction: 9,670
Total: 11,358

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.