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- W4298840488 abstract "The Food and Drug Administration (FDA) is announcing that it has issued an order in the form of a letter to a petitioner reclassifying the magnetic resonance diagnostic device, from class III (premarket approval) into class II (performance standards). The order is being codified in the Code of Federal Regulations as specified herein." @default.
- W4298840488 created "2022-10-02" @default.
- W4298840488 date "1989-02-01" @default.
- W4298840488 modified "2023-09-29" @default.
- W4298840488 title "Magnetic resonance diagnostic device; panel recommendation and report on petitions for magnetic resonance reclassification and codification of reclassification--FDA. Final rule." @default.
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