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In a recent JAMA MEDICAL NEWS story on premarket approval of class III medical devices by the Food and Drug Administration (242:2749-2753, 1979), the name of one device was incorrectly spelled and the manufacturer's name was incorrectly given.
The biochemical test to detect Neisseria gonorrhoeae in male urethral discharge is Gonodecten, and it is manufactured by the United States Packaging Corp Inc, Medical Products Division, La Porte, Ind.
Correction. JAMA. 1980;243(7):631. doi:10.1001/jama.1980.03300330009008