RADIFOCUS(R) (CATHETER) GUIDE WIRE— 510(k) K924202

Substantially Equivalent

Terumo Medical Corp.

FDA 510(k) clearance K924202 for RADIFOCUS(R) (CATHETER) GUIDE WIRE, Substantially Equivalent on 1992-11-23. Applicant: Terumo Medical Corp..

Clearance details

Applicant: Terumo Medical Corp.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 1992-08-20
Decision date: 1992-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elkton, MD, US

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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.