QLAB QUANTIFICATION SOFTWARE— 510(k) K132165

Substantially Equivalent

Philips Ultrasound, Inc.

FDA 510(k) clearance K132165 for QLAB QUANTIFICATION SOFTWARE, Substantially Equivalent on 2013-08-09. Applicant: Philips Ultrasound, Inc..

Clearance details

Applicant: Philips Ultrasound, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2013-07-12
Decision date: 2013-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.