Seyen Intl., Inc.
PROTEX LATEX EXAMINATION GLOVE
SKU K900790UPC LYY
In Stock
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IFDA 510(k) Cleared (K900790)
1
Free shipping on orders over $99 · 30-day returns
Seyen Intl., Inc.
Free shipping on orders over $99 · 30-day returns
PROTEX LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K900790) manufactured by Seyen Intl., Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 4, 1990. Regulation: 8.
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