Kadir Hi-Torque Guide Wire

by Argon Medical Corp. 510(k)

Active United States

510(k) K871297

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK871297	Date10 Apr 1987Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K871297
FDA Product Code: KOD

Device Class: Class II
Regulation: 21 CFR Part 876.5130
Advisory Committee: Gastroenterology, Urology
FDA Decision: SESE Substantially Equivalent

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