9th Wave, Inc.
9TH WAVE MODEL 200 ALTERNATING PRESSURE PAD
SKU K963677UPC FNM
In Stock
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IIFDA 510(k) Cleared (K963677)
1
Free shipping on orders over $99 · 30-day returns
9th Wave, Inc.
Free shipping on orders over $99 · 30-day returns
9TH WAVE MODEL 200 ALTERNATING PRESSURE PAD is an FDA 510(k)-cleared medical device (K963677) manufactured by 9th Wave, 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 November 25, 1996. Regulation: 8.
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