K-number	K223254
Device name	C2 Xplore
Applicant	Inomed Medizintechnik GmbH
Product code	ETN
Device class	Class II
Decision date	Jan 27, 2023
Decision	Substantially Equivalent
Regulation	874.1820

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Source

View the full FDA submission: accessdata.fda.gov

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C2 Xplore

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