K173378

Substantially Equivalent

syngo®.via protoNeo (Version VA20)

Applicant: Siemens Healthcare GmbH
Product code: LLZ
Advisory panel: Radiology
Date received: 2017-10-30
Decision date: 2017-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erlangen, DE

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.