
Yty Industry (Manjung) Sdn Bhd
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EVERGREEN NON-STERILE POWDERED LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K974191) manufactured by Yty Industry (Manjung) Sdn Bhd. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 23, 1997. Regulation: 8.

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