K-number	K240434
Device name	RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)
Applicant	Li Medical Corporation , Ltd.
Product code	HHK
Device class	Class II
Decision date	Sep 25, 2024
Decision	Substantially Equivalent
Regulation	884.1175

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View the full FDA submission: accessdata.fda.gov

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RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)

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