EchoNavigator R4.0— 510(k) K221270

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K221270 for EchoNavigator R4.0, Substantially Equivalent on 2022-05-31. Applicant: Philips Medical Systems Nederland B.V..

Clearance details

Applicant: Philips Medical Systems Nederland B.V.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2022-05-02
Decision date: 2022-05-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Best, NL

Download summary PDF View on FDA.gov ↗

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.