KENKOWAVE INFRARED PAIN TREATMENT SYSTEM— 510(k) K033555

Substantially Equivalent

Kaylight Corporation

FDA 510(k) clearance K033555 for KENKOWAVE INFRARED PAIN TREATMENT SYSTEM, Substantially Equivalent on 2004-03-02. Applicant: Kaylight Corporation.

Clearance details

Applicant: Kaylight Corporation
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2003-11-12
Decision date: 2004-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodbury, CT, US

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

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.