What role does FDA play on lasers?
The FDA regulates medical and non-medical lasers. The FDA may inspect the manufacturers of laser products and require the recall of products that do not meet federal standards or have radiation safety defects. The agency can also test laser products and check the display of laser displays to ensure that the public is protected. Producers of laser shows must tell the FDA where they plan to hold an exhibition so that the agency can inspect it if possible and take action when needed.
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The reason for the US FDA’s warning is that some irresponsible parents use laser pointers as toys for their children. There is a great risk. If the children aim the laser at the surface of a reflective object, the reflected beam may be more The beam originally emitted is more intense. The FDA requires labels to be placed on most laser products, warns of laser radiation and other hazards, and issues a statement that the blue laser pointer complies with FDA safety regulations. The label must also state the power output and hazard category of the product. Consumer laser products are generally classified into Class I, Class II and Class IIIa, while lasers for professional use can be classified into Class III b and Class IV.
2021-10-15 08:38:00
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