
Roche Diagnostic Systems, Inc.
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ROCHE COBAS INTEGRA REAGENT CASSETTES & ANCILLARY REAGENTS is an FDA 510(k)-cleared medical device (K972250) manufactured by Roche Diagnostic Systems, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1997. Regulation: 8.