K-number	K233751
Device name	Milieve (YPS-301BD)
Applicant	Soterix Medical, Inc.
Product code	PCC
Device class	Class II
Decision date	Jun 3, 2024
Decision	Substantially Equivalent
Regulation	882.5891

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Source

View the full FDA submission: accessdata.fda.gov

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Milieve (YPS-301BD)

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