Boehringer Mannheim Corp.
SOFTTOUCH II LANCET DEVICE
SKU K931258UPC FMK
In Stock
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IIFDA 510(k) Cleared (K931258)
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Free shipping on orders over $99 · 30-day returns
Boehringer Mannheim Corp.
Free shipping on orders over $99 · 30-day returns
SOFTTOUCH II LANCET DEVICE is an FDA 510(k)-cleared medical device (K931258) manufactured by Boehringer Mannheim Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 9, 1994. Regulation: 8.
