
General Physiotherapy, Inc.
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NEOCUSSOR (MASSAGER, BATTERY) POWERED is an FDA 510(k)-cleared medical device (K855129) manufactured by General Physiotherapy, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 1986. Regulation: 8.

ADC
SKU DX606933

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