K-number	K963580
Device name	IMAGYN FALLOPOSCOPY SYSTEM
Applicant	Imagyn Medical, Inc.
Product code	MKO
Device class	Class II
Decision date	Jan 31, 1997
Decision	Substantially Equivalent
Regulation	884.1690

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View the full FDA submission: accessdata.fda.gov

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IMAGYN FALLOPOSCOPY SYSTEM

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