
Rocap Div. of Sabratek Corp.
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ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML is an FDA 510(k)-cleared medical device (K990308) manufactured by Rocap Div. of Sabratek 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 December 9, 1999. Regulation: 8.

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