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2). Is Your Doctor's Hair Removal Laser Safe? By : Doug Smith
The U.S. Food and Drug Administration (FDA) regulates medical devices in the U.S. The FDA keeps extensive databases on these devices containing lists of the devices, their safety records, pre-market notifications, and pre-market approval notices, to name a few.
Section 510(k) of the Food, Drug and Cosmetic Act requires regulated medical device manufacturers to notify the FDA at least 90 days in advance of their intent to market a medical device.
Article Related to: laser, hair, removal, medical, lasers, devices, fda, regulation, 510(k)
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