PHILIPS DIGITAL IMAGING OPTION RELEASE 1— 510(k) K023440

Substantially Equivalent

Philips Medical Systems

FDA 510(k) clearance K023440 for PHILIPS DIGITAL IMAGING OPTION RELEASE 1, Substantially Equivalent on 2002-10-30. Applicant: Philips Medical Systems.

Clearance details

Applicant: Philips Medical Systems
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2002-10-15
Decision date: 2002-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, 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.