K-number	K920633
Device name	PESSARY FLEXIBLE SILICONE NICHOLS
Applicant	Bioteque America, Inc.
Product code	KXP
Device class	Class II
Decision date	Nov 8, 1995
Decision	Substantially Equivalent
Regulation	884.3900

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View the full FDA submission: accessdata.fda.gov

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PESSARY FLEXIBLE SILICONE NICHOLS

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