MOBILE X-RAY SYSTEM— 510(k) K913525

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K913525 for MOBILE X-RAY SYSTEM, Substantially Equivalent on 1991-10-23. Applicant: Siemens Medical Solutions USA, Inc..

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code OXO
Advisory panel: Radiology
Date received: 1991-08-08
Decision date: 1991-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

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Adverse events under product code OXO

product code OXO

Death: 6
Injury: 163
Malfunction: 2,099
Other: 1
Total: 2,269

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.