K-number	K771211
Device name	DOPPLER (UTD-5 & UTD-6)
Applicant	Terumo America, Inc.
Product code	HEK
Device class	Class II
Decision date	Jul 14, 1977
Decision	Substantially Equivalent
Regulation	884.2660

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View the full FDA submission: accessdata.fda.gov

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DOPPLER (UTD-5 & UTD-6)

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