
Amersham Corp.
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AMERLITE PROGESTERONE ASSAY, LAN.0079/2079 240/144 is an FDA 510(k)-cleared medical device (K884100) manufactured by Amersham Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 9, 1988. Regulation: 8.