Quinton, Inc.
MODIFIED SUTURE USED IN CATHETER INSERTION TRAYS
SKU K892450UPC KGX
In Stock
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IFDA 510(k) Cleared (K892450)
1
Free shipping on orders over $99 · 30-day returns
Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED SUTURE USED IN CATHETER INSERTION TRAYS is an FDA 510(k)-cleared medical device (K892450) manufactured by Quinton, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 10, 1989. Regulation: 8.
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