Columbus Dental Mfg. Co.
DRI-CLAVE LIQUID KLEENZALL
SKU K880754UPC EHZ
In Stock
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IFDA 510(k) Cleared (K880754)
1
Free shipping on orders over $99 · 30-day returns
Columbus Dental Mfg. Co.
Free shipping on orders over $99 · 30-day returns
DRI-CLAVE LIQUID KLEENZALL is an FDA 510(k)-cleared medical device (K880754) manufactured by Columbus Dental Mfg. Co.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 11, 1988. Regulation: 8.
