K-number	K922669
Device name	MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW
Applicant	Koven and Assoc., Inc.
Product code	DPW
Device class	Class II
Decision date	Jan 29, 1993
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW

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