Lyphomed, Inc.
SPARK KIT(R), MODIFICATION
SKU K910142UPC FPA
In Stock
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IIFDA 510(k) Cleared (K910142)
1
Free shipping on orders over $99 · 30-day returns
Lyphomed, Inc.
Free shipping on orders over $99 · 30-day returns
SPARK KIT(R), MODIFICATION is an FDA 510(k)-cleared medical device (K910142) manufactured by Lyphomed, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 13, 1991. Regulation: 8.
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