FDA 510(k) Applications Submitted by KEN JARRELL

FDA 510(k) Number Submission Date Device Name Applicant
K060410 02/16/2006 ECHOHEART TRANSVAGINAL DOPPLER PROBE SUMMIT DOPPLER SYSTEMS, INC.
K090499 02/25/2009 LIFEDOP MODEL, L350R SUMMIT DOPPLER SYSTEMS, INC.
K101816 06/30/2010 STN PROBE SUMMIT DOPPLER SYSTEMS, INC.
K093393 10/30/2009 LIFEDOP MODEL 300ABI SUMMIT DOPPLER SYSTEMS, INC.
K063600 12/04/2006 VISTA AVS SUMMIT DOPPLER SYSTEMS, INC.
K103693 12/17/2010 VANTAGE ABI SUMMIT DOPPLER SYSTEMS, INC.
K024197 12/20/2002 LIFEDOP DOPPLER SUMMIT DOPPLER SYSTEMS, INC.


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