K-number	K222798
Device name	Rejoni Intrauterine Catheter
Applicant	Rejoni, Inc.
Product code	LKF
Device class	Class II
Decision date	Dec 16, 2022
Decision	Substantially Equivalent
Regulation	884.4530

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Source

View the full FDA submission: accessdata.fda.gov

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Rejoni Intrauterine Catheter

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