K-number	K172752
Device name	CELERITY 20 HP Biological Indicator
Applicant	STERIS Corporation
Product code	FRC
Device class	Class II
Decision date	Feb 9, 2018
Decision	Substantially Equivalent
Regulation	880.2800

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Source

View the full FDA submission: accessdata.fda.gov

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CELERITY 20 HP Biological Indicator

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