K-number	K924631
Device name	CABOT MEDICAL UTERINE RESECTOSCOPE
Applicant	Cabot Medical Corp.
Product code	HIH
Device class	Class II
Decision date	May 16, 1994
Decision	Substantially Equivalent
Regulation	884.1690

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View the full FDA submission: accessdata.fda.gov

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CABOT MEDICAL UTERINE RESECTOSCOPE

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