K-number	K182764
Device name	Biop Digital Colposcope
Applicant	Biop Medical , Ltd.
Product code	HEX
Device class	Class II
Decision date	Nov 27, 2018
Decision	Substantially Equivalent
Regulation	884.1630

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View the full FDA submission: accessdata.fda.gov

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Biop Digital Colposcope

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