K-number	K183301
Device name	PRO-LITE Sterilization Tray
Applicant	STERIS Corporation
Product code	KCT
Device class	Class II
Decision date	Jan 3, 2019
Decision	Substantially Equivalent
Regulation	880.6850

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Source

View the full FDA submission: accessdata.fda.gov

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PRO-LITE Sterilization Tray

Everything you need for a 510(k) submission. Nothing you don't.