
K-Jump Health Co., Ltd.
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COMPRESSOR NEBULIZER SYSTEM, MODEL KN-9321 is an FDA 510(k)-cleared medical device (K051365) manufactured by K-Jump Health Co., Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 21, 2005. Regulation: 8.