Dlp, Inc.
MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.
SKU K896019UPC GAA
In Stock
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IFDA 510(k) Cleared (K896019)
1
Free shipping on orders over $99 · 30-day returns
Dlp, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. is an FDA 510(k)-cleared medical device (K896019) manufactured by Dlp, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 2, 1990. Regulation: 8.
