
In Vitro Diagnostics, Inc.
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LITHIUM INTERNAL STANDARD 1500 MEQ/L #60086 is an FDA 510(k)-cleared medical device (K871188) manufactured by In Vitro Diagnostics, 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 May 27, 1987. Regulation: 8.