KINETDX— 510(k) K041029

Substantially Equivalent

Siemens Medi Cal Solutions, Inc.

FDA 510(k) clearance K041029 for KINETDX, Substantially Equivalent on 2004-07-08. Applicant: Siemens Medi Cal Solutions, Inc..

Clearance details

Applicant: Siemens Medi Cal Solutions, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2004-04-21
Decision date: 2004-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ann Arbor, MI, 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.