K-number	K001677
Device name	BABY DOPPLEX 4000 (BD4000)
Applicant	Huntleigh Diagnostics , Ltd.
Product code	HGM
Device class	Class II
Decision date	Aug 14, 2000
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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BABY DOPPLEX 4000 (BD4000)

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