QT Ultrasound Breast Scanner-1— 510(k) K162372

Substantially Equivalent

Qt Ultrasound, LLC

FDA 510(k) clearance K162372 for QT Ultrasound Breast Scanner-1, Substantially Equivalent on 2017-06-06. Applicant: Qt Ultrasound, LLC.

Clearance details

Applicant
Qt Ultrasound, LLC
Product code
Code IYO
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Novato, CA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code IYO

product code IYO
Malfunction
3,339
Total
3,339

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 →

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