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- W2022689208 abstract "The Food and Drug Administration has moved to restrict the use of a particular type of intraocular lens implant—the anterior chamber angle support lens— despite the recent conclusion by a panel of expert ophthalmologists that this intraocular lens type and three others commonly used all yield significant visual advantages. (That appraisal was made this past fall at a consensus development conference on intraocular lenses sponsored by the National Institutes of Health [ JAMA (MEDICAL NEWS) 242:2047-2053, 1979].) In a statement, new FDA chief Jere Goyan, PhD, announced that only physicians who have implanted anterior chamber lenses in the past will be allowed to do so in the future. In addition, the agency will conduct special inspections of the plants where the anterior chamber lenses are made and will conduct its own laboratory analyses of the lenses. The anterior chamber lens is secured in the eye by wedging the device between the front" @default.
- W2022689208 created "2016-06-24" @default.
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- W2022689208 date "1980-01-04" @default.
- W2022689208 modified "2023-09-26" @default.
- W2022689208 title "FDA restricts use of one intraocular lens type" @default.
- W2022689208 doi "https://doi.org/10.1001/jama.1980.03300270006003" @default.
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