ALLURACLARITY XPER FD SERIES X-RAY SYSTEM— 510(k) K130638

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K130638 for ALLURACLARITY XPER FD SERIES X-RAY SYSTEM, Substantially Equivalent on 2013-06-28. Applicant: Philips Medical Systems Nederland B.V..

Clearance details

Applicant: Philips Medical Systems Nederland B.V.
Product code: Code OWB
Advisory panel: Radiology
Date received: 2013-03-11
Decision date: 2013-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Best, NL

Download summary PDF View on FDA.gov ↗

Adverse events under product code OWB

product code OWB

Death: 49
Injury: 340
Malfunction: 36,973
Total: 37,362

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.