Soliton, Inc.
Rapid Acoustic Pulse Device
SKU K201801UPC GEX
In Stock
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IIFDA 510(k) Cleared (K201801)
1
Free shipping on orders over $99 · 30-day returns
Soliton, Inc.
Free shipping on orders over $99 · 30-day returns
Rapid Acoustic Pulse Device is an FDA 510(k)-cleared medical device (K201801) manufactured by Soliton, 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 28, 2021. Regulation: 8.
