UMI STEERABLE TORQUE GUIDE WIRE— 510(k) K863178

Substantially Equivalent

Universal Medical Instrument Corp.

FDA 510(k) clearance K863178 for UMI STEERABLE TORQUE GUIDE WIRE, Substantially Equivalent on 1986-09-19. Applicant: Universal Medical Instrument Corp..

Clearance details

Applicant: Universal Medical Instrument Corp.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 1986-08-18
Decision date: 1986-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ballston Spa, NY, 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.