During a recent investigation by
the Idaho State Board of Medicine, it was determined that some
facilities are advertising and utilizing intense pulsed light
and/or laser devices for treatments such as hair removal.
The Medical Practice Act, Idaho Code §54-1804 0) creates an
exemption from medical licensure only with regard to the use of
Class I or Class II, non-prescriptive, approved, medical
devices.
The Center for Devices and Radiological Health of the Food
and Drug Administration (FDA) has classified intense pulsed
light and some laser devices as Class II prescriptive devices
and other laser devices as Class III devices. Class II intense
pulsed light/laser devices or Class III laser devices per FDA
requirements are sold to physicians only and are considered
prescriptive devices. Further information regarding FDA
requirements may be found at
http://www.fda.gov.