Trimedyne, Inc.
OMNIPULSE/OMNIPULSE-MAX
SKU K962632UPC GEX
In Stock
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IIFDA 510(k) Cleared (K962632)
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Free shipping on orders over $99 · 30-day returns
Trimedyne, Inc.
Free shipping on orders over $99 · 30-day returns
OMNIPULSE/OMNIPULSE-MAX is an FDA 510(k)-cleared medical device (K962632) manufactured by Trimedyne, Inc.. 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 January 15, 1997. Regulation: 8.
