We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » U.S. FDA Releases Guidance, Rule on Low-Level Lasers
U.S. FDA Releases Guidance, Rule on Low-Level Lasers
May 2, 2011
The U.S. Food and Drug Administration (FDA) has released a guidance and final rule classifying low-level laser systems for aesthetic use into Class II with special controls.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor