K-number	K220920
Device name	Matreneu Percutaneous Balloon Compression Kit
Applicant	Shenzhen Shineyard Medical Device Co. , Ltd.
Product code	HAO
Device class	Class I
Decision date	Sep 7, 2022
Decision	Substantially Equivalent
Regulation	882.4535

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View the full FDA submission: accessdata.fda.gov

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Matreneu Percutaneous Balloon Compression Kit

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