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FDA 510(k) Applications Submitted by SUMMIT DOPPLER SYSTEMS, INC.
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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