K-number	K871383
Device name	FETALERT ADR FETAL MONITOR
Applicant	Advanced Technology Laboratories, Inc.
Product code	HGM
Device class	Class II
Decision date	Jun 1, 1987
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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FETALERT ADR FETAL MONITOR

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