K-number	K911844
Device name	HYSTEROFLATOR 1500
Applicant	F.M. Wiest USA, Inc.
Product code	HIG
Device class	Class II
Decision date	Nov 21, 1991
Decision	Substantially Equivalent
Regulation	884.1700

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View the full FDA submission: accessdata.fda.gov

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HYSTEROFLATOR 1500

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