VERISUITE 1.6, VERISUITE-PARTICLE 1.6— 510(k) K080742

Substantially Equivalent

Medcom GmbH

FDA 510(k) clearance K080742 for VERISUITE 1.6, VERISUITE-PARTICLE 1.6, Substantially Equivalent on 2008-05-09. Applicant: Medcom GmbH.

Clearance details

Applicant: Medcom GmbH
Product code: Code IYE
Advisory panel: Radiology
Date received: 2008-03-17
Decision date: 2008-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Darmstadt, Hessen, DE

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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.