K-number	K010889
Device name	BABY DOPPLEX 3000 MK 2 (BD3000)
Applicant	Huntleigh Healthcare, Inc.
Product code	HGM
Device class	Class II
Decision date	Apr 25, 2001
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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BABY DOPPLEX 3000 MK 2 (BD3000)

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