Kaylight Corporation
KENKOWAVE INFRARED PAIN TREATMENT SYSTEM
SKU K033555UPC ILY
In Stock
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IIFDA 510(k) Cleared (K033555)
1
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Kaylight Corporation
Free shipping on orders over $99 · 30-day returns
KENKOWAVE INFRARED PAIN TREATMENT SYSTEM is an FDA 510(k)-cleared medical device (K033555) manufactured by Kaylight Corporation. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 1, 2004. Regulation: 8.
