K253871

Klär Lite (RCW-KL1000)

510(k) number
K253871
Device name
Klär Lite (RCW-KL1000)
Applicant
Radcliffe Watts, LLC OH · US
Product code
FTC — Light, Ultraviolet, Dermatological
Decision date
2026-03-04
Date received
2025-12-04
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
General, Plastic Surgery
510(k) Summary (official FDA PDF): K253871.pdf
Official FDA record: K253871
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.