K-number	K060320
Device name	FEMECC ENDOCERVICAL CURETTE
Applicant	Femspec LLC
Product code	PCF
Device class	Class II
Decision date	Jul 28, 2006
Decision	Substantially Equivalent
Regulation	884.1050

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View the full FDA submission: accessdata.fda.gov

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FEMECC ENDOCERVICAL CURETTE

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