AQUILION ONE— 510(k) K113466

Substantially Equivalent

Toshiba Medical Systems Coporation, Japan

FDA 510(k) clearance K113466 for AQUILION ONE, Substantially Equivalent on 2012-04-10. Applicant: Toshiba Medical Systems Coporation, Japan. Device class: 2.

Clearance details

Applicant
Toshiba Medical Systems Coporation, Japan
Product code
Code JAK
Device class
Class 2
Regulation
21 CFR 892.1750
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Tustin, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code JAK

view all

More clearances from Toshiba Medical Systems Coporation, Japan

view all

Adverse events under product code JAK

product code JAK
Death
27
Injury
571
Malfunction
779
Total
1,377

Source: openFDA MAUDE database, through . 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 K113466

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 K113466.

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