MEVATRON KD-2— 510(k) K862339

Substantially Equivalent

Siemens Medical Laboratories, Inc.

FDA 510(k) clearance K862339 for MEVATRON KD-2, Substantially Equivalent on 1986-10-29. Applicant: Siemens Medical Laboratories, Inc..

Clearance details

Applicant: Siemens Medical Laboratories, Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 1986-06-20
Decision date: 1986-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walnut Creek, CA, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

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.