VISIOFOCUS— 510(k) K122412

Substantially Equivalent

Tecnimed S.R.L.

FDA 510(k) clearance K122412 for VISIOFOCUS, Substantially Equivalent on 2013-03-13. Applicant: Tecnimed S.R.L..

Clearance details

Applicant: Tecnimed S.R.L.
Product code: Code FLL
Advisory panel: General Hospital
Date received: 2012-08-08
Decision date: 2013-03-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Ormond Beach, FL, US

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Adverse events under product code FLL

product code FLL

Death: 3
Malfunction: 557
Total: 560

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.