INTERA-SENSATION FAMILY— 510(k) K031815

Substantially Equivalent

Philips Medical Systems

FDA 510(k) clearance K031815 for INTERA-SENSATION FAMILY, Substantially Equivalent on 2003-09-10. Applicant: Philips Medical Systems.

Clearance details

Applicant: Philips Medical Systems
Product code: Code LNH
Advisory panel: Radiology
Date received: 2003-06-12
Decision date: 2003-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

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.