Jeanine Alcantara Intl.
PATIENT EXAMINATION GLOVE (LATEX)
SKU K891979UPC LYY
In Stock
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IFDA 510(k) Cleared (K891979)
1
Free shipping on orders over $99 · 30-day returns
Jeanine Alcantara Intl.
Free shipping on orders over $99 · 30-day returns
PATIENT EXAMINATION GLOVE (LATEX) is an FDA 510(k)-cleared medical device (K891979) manufactured by Jeanine Alcantara Intl.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 27, 1989. Regulation: 8.
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