LIFECLINIC, MODEL 2400— 510(k) K040562

Substantially Equivalent

Lifeclinic International, Inc.

FDA 510(k) clearance K040562 for LIFECLINIC, MODEL 2400, Substantially Equivalent on 2004-08-31. Applicant: Lifeclinic International, Inc..

Clearance details

Applicant: Lifeclinic International, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2004-03-03
Decision date: 2004-08-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Hasbrouck Heights, NJ, US

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.