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Asahi Iryoki Co., Ltd.
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ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S is an FDA 510(k)-cleared medical device (K000740) manufactured by Asahi Iryoki Co., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2000. Regulation: 8.

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