K-number	K060410
Device name	ECHOHEART TRANSVAGINAL DOPPLER PROBE
Applicant	Summit Doppler Systems, Inc.
Product code	HEK
Device class	Class II
Decision date	Apr 10, 2006
Decision	Substantially Equivalent
Regulation	884.2660

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View the full FDA submission: accessdata.fda.gov

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ECHOHEART TRANSVAGINAL DOPPLER PROBE

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