K-number	K130778
Device name	DISCOSCOPES, CERVICAL ENDOSCOPES
Applicant	Rz Medizintechnik GmbH
Product code	HRX
Device class	Class II
Decision date	Apr 14, 2014
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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DISCOSCOPES, CERVICAL ENDOSCOPES

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