PALOMAR LIGHTCUBE— 510(k) K024179

Substantially Equivalent

Palomar Medical Products, Inc.

FDA 510(k) clearance K024179 for PALOMAR LIGHTCUBE, Substantially Equivalent on 2003-06-04. Applicant: Palomar Medical Products, Inc..

Clearance details

Applicant: Palomar Medical Products, Inc.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2002-12-18
Decision date: 2003-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cary, NC, US

Download summary PDF View on FDA.gov ↗

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.