K-number	K894415
Device name	DYMAX ENDOVAGINAL BIOPSY GUIDE
Applicant	Dymax Corp
Product code	HGL
Device class	Class II
Decision date	Oct 25, 1989
Decision	Substantially Equivalent
Regulation	884.2960

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View the full FDA submission: accessdata.fda.gov

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DYMAX ENDOVAGINAL BIOPSY GUIDE

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