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This article was originally published in Clinica
The US FDA will review Cygnus' premarket approval (PMA) application for the GlucoWatch automatic, non-invasive glucose monitor under expedited review status. This is given to technology which is seen as in the public's health interest and therefore a priority for approval. Redwood City, California-based Cygnus submitted the final module of its PMA last month (see Clinica No 861, p 17).
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