BRANSIST SAFIRE— 510(k) K062360

Name: FDA 510(k) clearance K062360
Creator: U.S. Food and Drug Administration
Published: 2006-10-05

Substantially Equivalent

Shimadzu Corp.

FDA 510(k) clearance K062360 for BRANSIST SAFIRE, Substantially Equivalent on 2006-10-05. Applicant: Shimadzu Corp.. Device class: 2.

Clearance details

Applicant: Shimadzu Corp.
Product code: Code IZI
Device class: Class 2
Regulation: 21 CFR 892.1600
Advisory panel: Radiology
Date received: 2006-08-14
Decision date: 2006-10-05
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IZI

product code IZI

Death: 9
Malfunction: 5,312
Total: 5,321

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 →

Recalls naming K062360

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K062360.

Data sourced from openFDA. This site is unofficial and independent of the FDA.