
Hazleton Research Products, Inc.
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DMEM & HAM'S F-12 (1:1) POWDERED MEDIUM is an FDA 510(k)-cleared medical device (K861886) manufactured by Hazleton Research Products, Inc.. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 28, 1986. Regulation: 8.