CANAMET : News August 24, 2004

CANAMET | Canadian National Medical Technologies

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FDA Marketing Clearance Received for PIESOMETER MK-1 TORONTO, August 24, 2004
CANAMET is pleased to announce that our PIESOMETER Mk-1, an ambulatory blood pressure monitoring system, has received 510k marketing clearance from the FDA (Food and Drug Administration, U.S. ) on August 24, 2004 . The 510k number for the PIESOMETER Mk-1 is K041169.
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