K-number	K222969
Device name	FERTI-LILY Conception Cup
Applicant	Rosesta Medical BV
Product code	HDR
Device class	Class II
Decision date	Jun 23, 2023
Decision	Substantially Equivalent
Regulation	884.5250

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Source

View the full FDA submission: accessdata.fda.gov

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FERTI-LILY Conception Cup

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