Quinton, Inc.
PERI-PATCH GLUE MOLD
SKU K810530UPC KGZ
In Stock
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IFDA 510(k) Cleared (K810530)
1
Free shipping on orders over $99 · 30-day returns
Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
PERI-PATCH GLUE MOLD is an FDA 510(k)-cleared medical device (K810530) manufactured by Quinton, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 23, 1981. Regulation: 8.
