K-number	K222052
Device name	VitroPRO
Applicant	CIVCO Medical Instruments Co., Inc.
Product code	ITX
Device class	Class II
Decision date	Nov 22, 2022
Decision	Substantially Equivalent
Regulation	892.1570

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Source

View the full FDA submission: accessdata.fda.gov

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VitroPRO

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