Biosound, Inc.
GENESIS III, (MOD. 7003/7004)
SKU K894370UPC DXK
In Stock
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IIFDA 510(k) Cleared (K894370)
1
Free shipping on orders over $99 · 30-day returns
Biosound, Inc.
Free shipping on orders over $99 · 30-day returns
GENESIS III, (MOD. 7003/7004) is an FDA 510(k)-cleared medical device (K894370) manufactured by Biosound, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 28, 1990. Regulation: 8.
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