
Terumo America, Inc.
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DISP. HYPODERMIC NEEDLE is an FDA 510(k)-cleared medical device (K771203) manufactured by Terumo America, Inc.. 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 July 13, 1977. Regulation: 8.

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