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VSM files blood pressure monitor with FDA:

This article was originally published in Clinica

Executive Summary

VSM MedTech has filed for FDA 510(k) clearance for its BPM-100 automated, non-invasive blood pressure monitor. The Vancouver, British Columbia-based company says it is confident that the product, designed for use in a doctor's office, will be cleared promptly by the FDA and plans to launch the device in the US in mid 2000. VSM is currently carrying out negotiations with various US companies on the distribution of the product.

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