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Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire

K250552 Class II Traditional
Decision Date
2025-07-25
Sponsor / Applicant
ABBOTT MEDICAL

Technical Specification

510(k) Submission ID K250552
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 2025-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire received FDA 510(k) clearance under submission number K250552, sponsored by ABBOTT MEDICAL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-07-25.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.