
Diagnostic Hybrids, Inc.
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FRESH CELLS MULTI-WELL PLATE CULTURES AND SHELL VIAL CULTURE is an FDA 510(k)-cleared medical device (K936271) manufactured by Diagnostic Hybrids, Inc.. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 25, 1994. Regulation: 8.