LIGHT RELIEF, MODEL LR150, LR200— 510(k) K070974

Substantially Equivalent

Light Relief, LLC

FDA 510(k) clearance K070974 for LIGHT RELIEF, MODEL LR150, LR200, Substantially Equivalent on 2007-05-24. Applicant: Light Relief, LLC.

Clearance details

Applicant: Light Relief, LLC
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2007-04-06
Decision date: 2007-05-24
Decision: Substantially Equivalent
Clearance type: Special
Location: Los Angeles, CA, 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.