MODIFICATION TO MEDSTATION— 510(k) K021934

Substantially Equivalent

Aisoftw@Re Medical, S.P.A.

FDA 510(k) clearance K021934 for MODIFICATION TO MEDSTATION, Substantially Equivalent on 2002-08-12. Applicant: Aisoftw@Re Medical, S.P.A..

Clearance details

Applicant: Aisoftw@Re Medical, S.P.A.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2002-06-12
Decision date: 2002-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Teaneck, NJ, 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.