K-number	K161554
Device name	ENDOFLATOR 40, ENDOFLATOR 50
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	HIF
Device class	Class II
Decision date	Mar 2, 2017
Decision	Substantially Equivalent
Regulation	884.1730

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Source

View the full FDA submission: accessdata.fda.gov

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ENDOFLATOR 40, ENDOFLATOR 50

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