
Beckman Instruments, Inc.
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PARAGON HEMOGLOBIN ELECTRO. REAG. KIT is an FDA 510(k)-cleared medical device (K802821) manufactured by Beckman Instruments, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 10, 1980. Regulation: 8.