K-number	K895763
Device name	ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING
Applicant	Healthdyne Cardiovascular, Inc.
Product code	KXO
Device class	Class II
Decision date	Dec 22, 1989
Decision	Substantially Equivalent
Regulation	884.2700

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View the full FDA submission: accessdata.fda.gov

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ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING

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