
Linton Biomed Corp.
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HEPARIN CAP, INJECTION CAP MALE LUER- is an FDA 510(k)-cleared medical device (K841772) manufactured by Linton Biomed Corp.. 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 5, 1984. Regulation: 8.

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