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FDA 510(k) Applications Submitted by PIERRE LEMIRE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071086
04/17/2007
RESOLUTIONMD CARDIAC PRODUCT FAMILY, MODEL: RELEASE 1.0
CALGARY SCIENTIFIC, INC.
K062164
07/28/2006
RESOLUTIONMD, VERSION 1.3
CALGARY SCIENTIFIC, INC.
K082693
09/15/2008
RESOLUTIONMD, RELEASE 2.1
CALGARY SCIENTIFIC, INC.
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