
Bentley Laboratories, Inc.
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QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q is an FDA 510(k)-cleared medical device (K903641) manufactured by Bentley Laboratories, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 8, 1990. Regulation: 8.