HI-TORQUE FLEX-T GUIDE WIRE, MODELS 1012067-01, 02, 03, 04 AND 05— 510(k) K083738

Substantially Equivalent

Abbott Vascular

FDA 510(k) clearance K083738 for HI-TORQUE FLEX-T GUIDE WIRE, MODELS 1012067-01, 02, 03, 04 AND 05, Substantially Equivalent on 2009-03-11. Applicant: Abbott Vascular.

Clearance details

Applicant: Abbott Vascular
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 2008-12-16
Decision date: 2009-03-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.