Radifocus Glidewire— 510(k) K152740

Name: FDA 510(k) clearance K152740
Creator: U.S. Food and Drug Administration
Published: 2015-11-16

Substantially Equivalent

Ashitaka Factory of Terumo Corp.

FDA 510(k) clearance K152740 for Radifocus Glidewire, Substantially Equivalent on 2015-11-16. Applicant: Ashitaka Factory of Terumo Corp.. Device class: 2.

Clearance details

Applicant: Ashitaka Factory of Terumo Corp.
Product code: Code DQX
Device class: Class 2
Regulation: 21 CFR 870.1330
Advisory panel: Cardiovascular
Date received: 2015-09-23
Decision date: 2015-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fujinomiya Shizuoka, JP

Download summary PDF View on FDA.gov ↗

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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.