RADIFOCUS GUIDE WIRE M— 510(k) K923607

Name: FDA 510(k) clearance K923607
Creator: U.S. Food and Drug Administration
Published: 1992-10-02

Substantially Equivalent

Terumo Medical Corp.

FDA 510(k) clearance K923607 for RADIFOCUS GUIDE WIRE M, Substantially Equivalent on 1992-10-02. Applicant: Terumo Medical Corp.. Device class: 2.

Clearance details

Applicant: Terumo Medical Corp.
Product code: Code KOD
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1992-07-16
Decision date: 1992-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elkton, MD, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KOD

product code KOD

Death: 5
Injury: 1,129
Malfunction: 7,019
Total: 8,153

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.