521.17 MARKETING CARTRIDGE-BASED ELECTRONIC NICOTINE DELIVERY SYSTEMS (ENDS) PRODUCTS AND OTHER ENDS PRODUCTS THAT HAVE NOT OBTAINED PREMARKET AUTHORIZATION.

No person shall market any cartridge-based electronic nicotine delivery systems (or ENDS) products and other ENDS products that has not obtained premarket authorization from the Food and Drug Administration (FDA) under section 910 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 387 through 387u).

(Ord. 72-2023. Passed 9-18-23.)

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