K-number	K191102
Device name	Precision S 4K Sinuscope
Applicant	Stryker
Product code	EOB
Device class	Class II
Decision date	Sep 6, 2019
Decision	Substantially Equivalent
Regulation	874.4760

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Source

View the full FDA submission: accessdata.fda.gov

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Precision S 4K Sinuscope

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