LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE— 510(k) K072048

Substantially Equivalent

Lynton Lasers Limited

FDA 510(k) clearance K072048 for LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE, Substantially Equivalent on 2007-11-16. Applicant: Lynton Lasers Limited.

Clearance details

Applicant: Lynton Lasers Limited
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2007-07-25
Decision date: 2007-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Holmes Chapel, Cheshire, GB

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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.