LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109— 510(k) K073260

Substantially Equivalent

Device Partners International

FDA 510(k) clearance K073260 for LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109, Substantially Equivalent on 2008-03-13. Applicant: Device Partners International.

Clearance details

Applicant: Device Partners International
Product code: Code DTL
Advisory panel: Cardiovascular
Date received: 2007-11-20
Decision date: 2008-03-13
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Winston-Salem, NC, US

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Adverse events under product code DTL

product code DTL

Malfunction: 770
Total: 770

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.