K-number	K901592
Device name	MODEL MD-5 DOPPLER
Applicant	D. E. Hokanson, Inc.
Product code	DXK
Device class	Class II
Decision date	Oct 22, 1990
Decision	Substantially Equivalent
Regulation	870.2330

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View the full FDA submission: accessdata.fda.gov

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MODEL MD-5 DOPPLER

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