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Zdrowie i gospodarka · 18.02.2015

Immediately in Effect Guidance Document: Classification and Requirements for Laser Illuminated Projectors; Guidance for Industry and Food and Drug Administration Staff; Availability

The Food and Drug Administration (FDA) is announcing the availability of the guidance entitled "Immediately in Effect Guidance Document: Classification and Requirements for Laser Illuminated Projectors (LIPs)." This guidance describes FDA's policy with respect to certain LIPs that comply with International Electrotechnical Commission (IEC) standards during laser product classification under the Electronic Product Radiation Control provisions of the Federal Food, Drug and Cosmetic Act (the FD&C Act) that apply to electronic products.

Source: Federal Register — Food and Drug AdministrationOpen original release →