K-number	K191594
Device name	Nuvis Battery Arthroscope
Applicant	Integrated Endoscopy, Inc.
Product code	HRX
Device class	Class II
Decision date	Jul 11, 2019
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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Nuvis Battery Arthroscope

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