
Sigma Diagnostics, Inc.
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ALKALINE PHOSPHATASE (ALP/AMP) PROCEDURE NO. 247 is an FDA 510(k)-cleared medical device (K951584) manufactured by Sigma 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 August 10, 1995. Regulation: 8.