
Asia Way Trading, Inc.
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NON-STERILE PATIENT EXAMINATION GLOVES (LATEX) is an FDA 510(k)-cleared medical device (K892747) manufactured by Asia Way Trading, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 21, 1989. Regulation: 8.

Ansell
SKU MSC846624

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SKU K014192

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SKU VM-1270030

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SKU VM-1270031