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Summit Doppler Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103693VANTAGE ABIFebruary 15, 2011
K101816STN PROBEAugust 19, 2010
K093393LIFEDOP MODEL 300ABIDecember 24, 2009
K090499LIFEDOP MODEL, L350RMarch 31, 2009
K063600VISTA AVSDecember 19, 2006
K060410ECHOHEART TRANSVAGINAL DOPPLER PROBEApril 10, 2006
K024197LIFEDOP DOPPLERJanuary 3, 2003