MICROLIFE IT2CA1— 510(k) K990168

Substantially Equivalent

Microlife Systems AG

FDA 510(k) clearance K990168 for MICROLIFE IT2CA1, Substantially Equivalent on 1999-02-25. Applicant: Microlife Systems AG.

Clearance details

Applicant: Microlife Systems AG
Product code: Code FLL
Advisory panel: General Hospital
Date received: 1999-01-19
Decision date: 1999-02-25
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Leesburg, 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.