PHILIPS INTURIS DICOM RECORDER— 510(k) K993227

Substantially Equivalent

Philips Medical Systems North America, Inc.

FDA 510(k) clearance K993227 for PHILIPS INTURIS DICOM RECORDER, Substantially Equivalent on 1999-12-21. Applicant: Philips Medical Systems North America, Inc..

Clearance details

Applicant: Philips Medical Systems North America, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1999-09-27
Decision date: 1999-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, CT, 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.