CAREMATIX WELLNESS SYSTEM— 510(k) K031840

Substantially Equivalent

Carematix, Inc.

FDA 510(k) clearance K031840 for CAREMATIX WELLNESS SYSTEM, Substantially Equivalent on 2003-10-10. Applicant: Carematix, Inc..

Clearance details

Applicant: Carematix, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2003-06-16
Decision date: 2003-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, 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.